ريفكا كارمي (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "ريفكا كارمي" in Arabic language version.

refsWebsite

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27web.archive.org

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21doi.org

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20worldcat.org

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20nih.gov

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9wiley.com

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4nature.com

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4haaretz.co.il

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2pnas.org

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2oxfordjournals.org

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2omim.org

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1bbc.com

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1karger.com

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1sciencemag.org

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1sciencedirect.com

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110.tv

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10.tv

"מבקר המדינה בודק הארכת מינויה של נשיאת אוניברסיטת בן גוריון". ערוץ עשר (بالعبرية). مؤرشف من الأصل في 2018-02-07. اطلع عليه بتاريخ 2018-02-06.

bbc.com

https://www.bbc.com/news/world-34745739. اطلع عليه بتاريخ 2022-12-17. {{استشهاد ويب}}: |url= بحاجة لعنوان (مساعدة) والوسيط |title= غير موجود أو فارغ (من ويكي بيانات) (مساعدة)

doi.org

Raz، Aviad E.؛ Atar، Marcela؛ Rodnay، Maya؛ Shoham-Vardi، Ilana؛ Carmi، Rivka. "Between Acculturation and Ambivalence: Knowledge of Genetics and Attitudes towards Genetic Testing in a Consanguineous Bedouin Community". Public Health Genomics. ج. 6 ع. 2: 88–95. DOI:10.1159/000073004. مؤرشف من الأصل في 2020-03-14.
Birnbaum, Ramon Y.; Landau, Daniella; Elbedour, Khalil; Ofir, Rivka; Birk, Ohad S.; Carmi, Rivka (15 Apr 2008). "Deletion of the first pair of fibronectin type III repeats of the integrin β-4 gene is associated with epidermolysis bullosa, pyloric atresia and aplasia cutis congenita in the original Carmi syndrome patients". American Journal of Medical Genetics Part A (بالإنجليزية). 146A (8): 1063–1066. DOI:10.1002/ajmg.a.31903. ISSN:1552-4833. Archived from the original on 2017-12-01.
Chiang, Annie P.; Beck, John S.; Yen, Hsan-Jan; Tayeh, Marwan K.; Scheetz, Todd E.; Swiderski, Ruth E.; Nishimura, Darryl Y.; Braun, Terry A.; Kim, Kwang-Youn A. (18 Apr 2006). "Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet–Biedl syndrome gene (BBS11)". Proceedings of the National Academy of Sciences (بالإنجليزية). 103 (16): 6287–6292. DOI:10.1073/pnas.0600158103. ISSN:0027-8424. PMC:1458870. PMID:16606853. Archived from the original on 2018-06-02.
Nishimura, Darryl Y.; Fath, Melissa; Mullins, Robert F.; Searby, Charles; Andrews, Michael; Davis, Roger; Andorf, Jeaneen L.; Mykytyn, Kirk; Swiderski, Ruth E. (23 Nov 2004). "Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin". Proceedings of the National Academy of Sciences of the United States of America (بالإنجليزية). 101 (47): 16588–16593. DOI:10.1073/pnas.0405496101. ISSN:0027-8424. PMC:534519. PMID:15539463. Archived from the original on 2018-11-05.
Mykytyn, Kirk; Nishimura, Darryl Y.; Searby, Charles C.; Shastri, Mythreyi; Yen, Hsan-jan; Beck, John S.; Braun, Terry; Streb, Luan M.; Cornier, Alberto S. (1 Aug 2002). "Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome". Nature Genetics (بالإنجليزية). 31 (4): 435–438. DOI:10.1038/ng935. ISSN:1061-4036. PMID:12118255. Archived from the original on 2006-04-11.
Walder, Roxanne Y.; Landau, Daniel; Meyer, Peter; Shalev, Hanna; Tsolia, Maria; Borochowitz, Zvi; Boettger, Melanie Barbara; Beck, Gretel E.; Englehardt, Richard K. (1 Jun 2002). "Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia". Nature Genetics (بالإنجليزية). 31 (2): 171–174. DOI:10.1038/ng901. ISSN:1061-4036. PMID:12032570. Archived from the original on 2010-10-23.
Nishimura, Darryl Y.; Searby, Charles C.; Carmi, Rivka; Elbedour, Khalil; Maldergem, Lionel Van; Fulton, Anne B.; Lam, Byron L.; Powell, Berkley R.; Swiderski, Ruth E. (2 Apr 2001). "Positional cloning of a novel gene on chromosome 16q causing Bardet–Biedl syndrome (BBS2)". Human Molecular Genetics (بالإنجليزية). 10 (8): 865–874. DOI:10.1093/hmg/10.8.865. ISSN:0964-6906. PMID:11285252. Archived from the original on 2016-05-17.
Haider, Neena B.; Jacobson, Samuel G.; Cideciyan, Artur V.; Swiderski, Ruth; Streb, Luan M.; Searby, Charles; Beck, Gretel; Hockey, Robin; Hanna, David B. (1 Feb 2000). "Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate". Nature Genetics (بالإنجليزية). 24 (2): 127–131. DOI:10.1038/72777. ISSN:1061-4036. PMID:10655056. Archived from the original on 2016-11-05.
Carstea, Eugene D.; Morris, Jill A.; Coleman, Katherine G.; Loftus, Stacie K.; Zhang, Dana; Cummings, Christiano; Gu, Jessie; Rosenfeld, Melissa A.; Pavan, William J. (11 Jul 1997). "Niemann-Pick C1 Disease Gene: Homology to Mediators of Cholesterol Homeostasis". Science (بالإنجليزية). 277 (5323): 228–231. DOI:10.1126/science.277.5323.228. ISSN:0036-8075. PMID:9211849. Archived from the original on 2017-12-15.
Maman, Eran; Maor, Esther; Kachko, Leonid; Carmi, Rivka (30 Jun 1998). "Epidermolysis bullosa, pyloric atresia, aplasia cutis congenita: Histopathological delineation of an autosomal recessive disease". American Journal of Medical Genetics (بالإنجليزية). 78 (2): 127–133. DOI:10.1002/(sici)1096-8628(19980630)78:2<127::aid-ajmg6>3.0.co;2-l. ISSN:1096-8628. Archived from the original on 2023-11-17.
Scott, Da; Kraft, Ml; Carmi, R; Ramesh, A; Elbedour, K; Yairi, Y; Srisailapathy, C. R. Srikumari; Rosengren, Ss; Markham, Af (1 Jan 1998). "Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss". Human Mutation (بالإنجليزية). 11 (5): 387–394. DOI:10.1002/(sici)1098-1004(1998)11:5<387::aid-humu6>3.0.co;2-8. ISSN:1098-1004. Archived from the original on 2022-05-17.
Buskila، Dan؛ Neumann، Lily؛ Hazanov، Ilia؛ Carmi، Rivka (1 ديسمبر 1996). "Familial aggregation in the fihromyalgia syndrome". Seminars in Arthritis and Rheumatism. ج. 26 ع. 3: 605–611. DOI:10.1016/S0049-0172(96)80011-4. مؤرشف من الأصل في 2020-03-28. {{استشهاد بدورية محكمة}}: |archive-date= / |archive-url= timestamp mismatch (مساعدة)
Carmi، R.؛ Rokhlina، T.؛ Kwitek-Black، A. E.؛ Elbedour، K.؛ Nishimura، D.؛ Stone، E. M.؛ Sheffield، V. C. (1 يناير 1995). "Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15". Human Molecular Genetics. ج. 4 ع. 1: 9–13. DOI:10.1093/hmg/4.1.9. ISSN:0964-6906. PMID:7711739.
Sheffield, Val C.; Carml, Rivka; Kwltek-Black, Anne; Rokhlina, Tatiana; Nishlmura, Darryl; Duyk, Geoffrey M.; Elbedour, Khalil; Sunden, Sara L.; Stone, Edwin M. (1 Aug 1994). "Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping". Human Molecular Genetics (بالإنجليزية). 3 (8): 1331–1335. DOI:10.1093/hmg/3.8.1331. ISSN:0964-6906. PMID:7987310. Archived from the original on 2020-04-14.
Carmi, R.; Gohar, J.; Meizner, I.; Katz, M. (1 Jun 1994). "Spontaneous abortion–high risk factor for neural tube defects in subsequent pregnancy". American Journal of Medical Genetics (بالإنجليزية). 51 (2): 93–97. DOI:10.1002/ajmg.1320510203. ISSN:1096-8628. Archived from the original on 2017-12-01.
Parvari, R.; Weinstein, Y.; Ehrlich, S.; Steinitz, M.; Carmi, R. (15 Feb 1994). "Linkage localization of the thoraco-abdominal syndrome (TAS) gene to Xq25–26". American Journal of Medical Genetics (بالإنجليزية). 49 (4): 431–434. DOI:10.1002/ajmg.1320490416. ISSN:1096-8628. PMID:7909197. Archived from the original on 2018-02-17.
Kwitek-Black, Anne E.; Carmi, Rivka; Duyk, Geoffrey M.; Buetow, Kenneth H.; Elbedour, Khalil; Parvari, Ruti; Yandava, Chandra Naidu; Stone, Edwin M.; Sheffield, Val C. (1 Dec 1993). "Linkage of Bardet–Biedl syndrome to chromosome 16q and evidence for non–allelic genetic heterogeneity". Nature Genetics (بالإنجليزية). 5 (4): 392–396. DOI:10.1038/ng1293-392. PMID:8298649. Archived from the original on 2015-01-28.
Carmi, Rivka; Boughman, Joann A. (1 Jan 1992). "Pentalogy of Cantrell and associated midline anomalies: A possible ventral midline developmental field". American Journal of Medical Genetics (بالإنجليزية). 42 (1): 90–95. DOI:10.1002/ajmg.1320420118. ISSN:1096-8628. PMID:1308371. Archived from the original on 2017-12-01.
Carmi, R.; Meizner, I.; Katz, M. (1 Jul 1990). "Familial congenital diaphragmatic defect and associated midline anomalies: Further evidence for an X-linked midline gene?". American Journal of Medical Genetics (بالإنجليزية). 36 (3): 313–315. DOI:10.1002/ajmg.1320360314. ISSN:1096-8628. PMID:2363430. Archived from the original on 2018-02-17.
Carmi, R.; Sofer, S.; Karplus, M.; Ben-Yakar, Y.; Mahler, D.; Zirkin, H.; Bar-Ziv, J.; Opitz, John M. (1 Mar 1982). "Aplasia cutis congenita in two sibs discordant for pylori atresia". American Journal of Medical Genetics (بالإنجليزية). 11 (3): 319–328. DOI:10.1002/ajmg.1320110308. ISSN:1096-8628. Archived from the original on 2017-12-01.
Carmi, R.; Barbash, A.; Mares, A. J. (1 May 1990). "The thoracoabdominal syndrome (TAS): A new X-linked dominant disorder". American Journal of Medical Genetics (بالإنجليزية). 36 (1): 109–114. DOI:10.1002/ajmg.1320360122. ISSN:1096-8628. PMID:2139758. Archived from the original on 2017-12-01.

haaretz.co.il

צור، ירדן (22 نوفمبر 2017). "חרף ההנחיות, אונ' בן גוריון רוצה להאריך את כהונת הנשיאה; הפרופסורים מתנגדים". הארץ (بالعبرية). مؤرشف من الأصل في 2017-12-01. اطلع عليه بتاريخ 2017-11-26.
צור، ירדן (21 ديسمبر 2017). "מחריף המשבר באונ' בן גוריון: נעצר הליך מינוי הרקטור החדש". הארץ (بالعبرية). مؤرشف من الأصل في 2018-02-07. اطلع عليه بتاريخ 2018-02-06.
(Tzur) צור، (Yarden) ירדן (2 يناير 2018). "(The president of Ben-Gurion University responds to the protest) נשיא אוניברסיטת בן גוריון מגיב למחאה". הארץ (بالعبرية). Ha'aretz. مؤرشف من الأصل في 2018-01-21. اطلع عليه بتاريخ 2018-01-21.
צור، ירדן (5 فبراير 2018). "אוניברסיטת בן גוריון: נבחר נשיא חדש עד תום 2018". הארץ (بالعبرية). مؤرشف من الأصل في 2018-05-08. اطلع عليه بتاريخ 2018-02-06.

karger.com

Raz، Aviad E.؛ Atar، Marcela؛ Rodnay، Maya؛ Shoham-Vardi، Ilana؛ Carmi، Rivka. "Between Acculturation and Ambivalence: Knowledge of Genetics and Attitudes towards Genetic Testing in a Consanguineous Bedouin Community". Public Health Genomics. ج. 6 ع. 2: 88–95. DOI:10.1159/000073004. مؤرشف من الأصل في 2020-03-14.

nature.com

Mykytyn, Kirk; Nishimura, Darryl Y.; Searby, Charles C.; Shastri, Mythreyi; Yen, Hsan-jan; Beck, John S.; Braun, Terry; Streb, Luan M.; Cornier, Alberto S. (1 Aug 2002). "Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome". Nature Genetics (بالإنجليزية). 31 (4): 435–438. DOI:10.1038/ng935. ISSN:1061-4036. PMID:12118255. Archived from the original on 2006-04-11.
Walder, Roxanne Y.; Landau, Daniel; Meyer, Peter; Shalev, Hanna; Tsolia, Maria; Borochowitz, Zvi; Boettger, Melanie Barbara; Beck, Gretel E.; Englehardt, Richard K. (1 Jun 2002). "Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia". Nature Genetics (بالإنجليزية). 31 (2): 171–174. DOI:10.1038/ng901. ISSN:1061-4036. PMID:12032570. Archived from the original on 2010-10-23.
Haider, Neena B.; Jacobson, Samuel G.; Cideciyan, Artur V.; Swiderski, Ruth; Streb, Luan M.; Searby, Charles; Beck, Gretel; Hockey, Robin; Hanna, David B. (1 Feb 2000). "Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate". Nature Genetics (بالإنجليزية). 24 (2): 127–131. DOI:10.1038/72777. ISSN:1061-4036. PMID:10655056. Archived from the original on 2016-11-05.
Kwitek-Black, Anne E.; Carmi, Rivka; Duyk, Geoffrey M.; Buetow, Kenneth H.; Elbedour, Khalil; Parvari, Ruti; Yandava, Chandra Naidu; Stone, Edwin M.; Sheffield, Val C. (1 Dec 1993). "Linkage of Bardet–Biedl syndrome to chromosome 16q and evidence for non–allelic genetic heterogeneity". Nature Genetics (بالإنجليزية). 5 (4): 392–396. DOI:10.1038/ng1293-392. PMID:8298649. Archived from the original on 2015-01-28.

nih.gov

pubmed.ncbi.nlm.nih.gov

Scott، D. A.؛ Carmi، R.؛ Elbedour، K.؛ Yosefsberg، S.؛ Stone، E. M.؛ Sheffield، V. C. (1 أغسطس 1996). "An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindreds". American Journal of Human Genetics. ج. 59 ع. 2: 385–391. ISSN:0002-9297. PMC:1914732. PMID:8755925.
Scott، D. A.؛ Carmi، R.؛ Elbedour، K.؛ Duyk، G. M.؛ Stone، E. M.؛ Sheffield، V. C. (1 أكتوبر 1995). "Nonsyndromic autosomal recessive deafness is linked to the DFNB1 locus in a large inbred Bedouin family from Israel". American Journal of Human Genetics. ج. 57 ع. 4: 965–968. ISSN:0002-9297. PMC:1801487. PMID:7573061.
Chiang, Annie P.; Beck, John S.; Yen, Hsan-Jan; Tayeh, Marwan K.; Scheetz, Todd E.; Swiderski, Ruth E.; Nishimura, Darryl Y.; Braun, Terry A.; Kim, Kwang-Youn A. (18 Apr 2006). "Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet–Biedl syndrome gene (BBS11)". Proceedings of the National Academy of Sciences (بالإنجليزية). 103 (16): 6287–6292. DOI:10.1073/pnas.0600158103. ISSN:0027-8424. PMC:1458870. PMID:16606853. Archived from the original on 2018-06-02.
Nishimura, Darryl Y.; Fath, Melissa; Mullins, Robert F.; Searby, Charles; Andrews, Michael; Davis, Roger; Andorf, Jeaneen L.; Mykytyn, Kirk; Swiderski, Ruth E. (23 Nov 2004). "Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin". Proceedings of the National Academy of Sciences of the United States of America (بالإنجليزية). 101 (47): 16588–16593. DOI:10.1073/pnas.0405496101. ISSN:0027-8424. PMC:534519. PMID:15539463. Archived from the original on 2018-11-05.
Mykytyn, Kirk; Nishimura, Darryl Y.; Searby, Charles C.; Shastri, Mythreyi; Yen, Hsan-jan; Beck, John S.; Braun, Terry; Streb, Luan M.; Cornier, Alberto S. (1 Aug 2002). "Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome". Nature Genetics (بالإنجليزية). 31 (4): 435–438. DOI:10.1038/ng935. ISSN:1061-4036. PMID:12118255. Archived from the original on 2006-04-11.
Walder, Roxanne Y.; Landau, Daniel; Meyer, Peter; Shalev, Hanna; Tsolia, Maria; Borochowitz, Zvi; Boettger, Melanie Barbara; Beck, Gretel E.; Englehardt, Richard K. (1 Jun 2002). "Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia". Nature Genetics (بالإنجليزية). 31 (2): 171–174. DOI:10.1038/ng901. ISSN:1061-4036. PMID:12032570. Archived from the original on 2010-10-23.
Nishimura, Darryl Y.; Searby, Charles C.; Carmi, Rivka; Elbedour, Khalil; Maldergem, Lionel Van; Fulton, Anne B.; Lam, Byron L.; Powell, Berkley R.; Swiderski, Ruth E. (2 Apr 2001). "Positional cloning of a novel gene on chromosome 16q causing Bardet–Biedl syndrome (BBS2)". Human Molecular Genetics (بالإنجليزية). 10 (8): 865–874. DOI:10.1093/hmg/10.8.865. ISSN:0964-6906. PMID:11285252. Archived from the original on 2016-05-17.
Haider, Neena B.; Jacobson, Samuel G.; Cideciyan, Artur V.; Swiderski, Ruth; Streb, Luan M.; Searby, Charles; Beck, Gretel; Hockey, Robin; Hanna, David B. (1 Feb 2000). "Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate". Nature Genetics (بالإنجليزية). 24 (2): 127–131. DOI:10.1038/72777. ISSN:1061-4036. PMID:10655056. Archived from the original on 2016-11-05.
Carstea, Eugene D.; Morris, Jill A.; Coleman, Katherine G.; Loftus, Stacie K.; Zhang, Dana; Cummings, Christiano; Gu, Jessie; Rosenfeld, Melissa A.; Pavan, William J. (11 Jul 1997). "Niemann-Pick C1 Disease Gene: Homology to Mediators of Cholesterol Homeostasis". Science (بالإنجليزية). 277 (5323): 228–231. DOI:10.1126/science.277.5323.228. ISSN:0036-8075. PMID:9211849. Archived from the original on 2017-12-15.
Carmi، R.؛ Rokhlina، T.؛ Kwitek-Black، A. E.؛ Elbedour، K.؛ Nishimura، D.؛ Stone، E. M.؛ Sheffield، V. C. (1 يناير 1995). "Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15". Human Molecular Genetics. ج. 4 ع. 1: 9–13. DOI:10.1093/hmg/4.1.9. ISSN:0964-6906. PMID:7711739.
Sheffield, Val C.; Carml, Rivka; Kwltek-Black, Anne; Rokhlina, Tatiana; Nishlmura, Darryl; Duyk, Geoffrey M.; Elbedour, Khalil; Sunden, Sara L.; Stone, Edwin M. (1 Aug 1994). "Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping". Human Molecular Genetics (بالإنجليزية). 3 (8): 1331–1335. DOI:10.1093/hmg/3.8.1331. ISSN:0964-6906. PMID:7987310. Archived from the original on 2020-04-14.
Parvari, R.; Weinstein, Y.; Ehrlich, S.; Steinitz, M.; Carmi, R. (15 Feb 1994). "Linkage localization of the thoraco-abdominal syndrome (TAS) gene to Xq25–26". American Journal of Medical Genetics (بالإنجليزية). 49 (4): 431–434. DOI:10.1002/ajmg.1320490416. ISSN:1096-8628. PMID:7909197. Archived from the original on 2018-02-17.
Kwitek-Black, Anne E.; Carmi, Rivka; Duyk, Geoffrey M.; Buetow, Kenneth H.; Elbedour, Khalil; Parvari, Ruti; Yandava, Chandra Naidu; Stone, Edwin M.; Sheffield, Val C. (1 Dec 1993). "Linkage of Bardet–Biedl syndrome to chromosome 16q and evidence for non–allelic genetic heterogeneity". Nature Genetics (بالإنجليزية). 5 (4): 392–396. DOI:10.1038/ng1293-392. PMID:8298649. Archived from the original on 2015-01-28.
Carmi, Rivka; Boughman, Joann A. (1 Jan 1992). "Pentalogy of Cantrell and associated midline anomalies: A possible ventral midline developmental field". American Journal of Medical Genetics (بالإنجليزية). 42 (1): 90–95. DOI:10.1002/ajmg.1320420118. ISSN:1096-8628. PMID:1308371. Archived from the original on 2017-12-01.
Carmi, R.; Meizner, I.; Katz, M. (1 Jul 1990). "Familial congenital diaphragmatic defect and associated midline anomalies: Further evidence for an X-linked midline gene?". American Journal of Medical Genetics (بالإنجليزية). 36 (3): 313–315. DOI:10.1002/ajmg.1320360314. ISSN:1096-8628. PMID:2363430. Archived from the original on 2018-02-17.
Carmi, R.; Barbash, A.; Mares, A. J. (1 May 1990). "The thoracoabdominal syndrome (TAS): A new X-linked dominant disorder". American Journal of Medical Genetics (بالإنجليزية). 36 (1): 109–114. DOI:10.1002/ajmg.1320360122. ISSN:1096-8628. PMID:2139758. Archived from the original on 2017-12-01.

ncbi.nlm.nih.gov

Scott، D. A.؛ Carmi، R.؛ Elbedour، K.؛ Yosefsberg، S.؛ Stone، E. M.؛ Sheffield، V. C. (1 أغسطس 1996). "An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindreds". American Journal of Human Genetics. ج. 59 ع. 2: 385–391. ISSN:0002-9297. PMC:1914732. PMID:8755925.
Scott، D. A.؛ Carmi، R.؛ Elbedour، K.؛ Duyk، G. M.؛ Stone، E. M.؛ Sheffield، V. C. (1 أكتوبر 1995). "Nonsyndromic autosomal recessive deafness is linked to the DFNB1 locus in a large inbred Bedouin family from Israel". American Journal of Human Genetics. ج. 57 ع. 4: 965–968. ISSN:0002-9297. PMC:1801487. PMID:7573061.
Chiang, Annie P.; Beck, John S.; Yen, Hsan-Jan; Tayeh, Marwan K.; Scheetz, Todd E.; Swiderski, Ruth E.; Nishimura, Darryl Y.; Braun, Terry A.; Kim, Kwang-Youn A. (18 Apr 2006). "Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet–Biedl syndrome gene (BBS11)". Proceedings of the National Academy of Sciences (بالإنجليزية). 103 (16): 6287–6292. DOI:10.1073/pnas.0600158103. ISSN:0027-8424. PMC:1458870. PMID:16606853. Archived from the original on 2018-06-02.
Nishimura, Darryl Y.; Fath, Melissa; Mullins, Robert F.; Searby, Charles; Andrews, Michael; Davis, Roger; Andorf, Jeaneen L.; Mykytyn, Kirk; Swiderski, Ruth E. (23 Nov 2004). "Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin". Proceedings of the National Academy of Sciences of the United States of America (بالإنجليزية). 101 (47): 16588–16593. DOI:10.1073/pnas.0405496101. ISSN:0027-8424. PMC:534519. PMID:15539463. Archived from the original on 2018-11-05.

omim.org

"OMIM - % 313850 - THORACOABDOMINAL SYNDROME; THAS". www.omim.org. مؤرشف من الأصل في 2019-04-25. اطلع عليه بتاريخ 2016-09-08.
"OMIM Entry - # 226730 - CARMI SYNDROME". www.omim.org. مؤرشف من الأصل في 2020-01-09. اطلع عليه بتاريخ 2016-09-08.

oxfordjournals.org

hmg.oxfordjournals.org

Nishimura, Darryl Y.; Searby, Charles C.; Carmi, Rivka; Elbedour, Khalil; Maldergem, Lionel Van; Fulton, Anne B.; Lam, Byron L.; Powell, Berkley R.; Swiderski, Ruth E. (2 Apr 2001). "Positional cloning of a novel gene on chromosome 16q causing Bardet–Biedl syndrome (BBS2)". Human Molecular Genetics (بالإنجليزية). 10 (8): 865–874. DOI:10.1093/hmg/10.8.865. ISSN:0964-6906. PMID:11285252. Archived from the original on 2016-05-17.
Sheffield, Val C.; Carml, Rivka; Kwltek-Black, Anne; Rokhlina, Tatiana; Nishlmura, Darryl; Duyk, Geoffrey M.; Elbedour, Khalil; Sunden, Sara L.; Stone, Edwin M. (1 Aug 1994). "Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping". Human Molecular Genetics (بالإنجليزية). 3 (8): 1331–1335. DOI:10.1093/hmg/3.8.1331. ISSN:0964-6906. PMID:7987310. Archived from the original on 2020-04-14.

pnas.org

Chiang, Annie P.; Beck, John S.; Yen, Hsan-Jan; Tayeh, Marwan K.; Scheetz, Todd E.; Swiderski, Ruth E.; Nishimura, Darryl Y.; Braun, Terry A.; Kim, Kwang-Youn A. (18 Apr 2006). "Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet–Biedl syndrome gene (BBS11)". Proceedings of the National Academy of Sciences (بالإنجليزية). 103 (16): 6287–6292. DOI:10.1073/pnas.0600158103. ISSN:0027-8424. PMC:1458870. PMID:16606853. Archived from the original on 2018-06-02.
Nishimura, Darryl Y.; Fath, Melissa; Mullins, Robert F.; Searby, Charles; Andrews, Michael; Davis, Roger; Andorf, Jeaneen L.; Mykytyn, Kirk; Swiderski, Ruth E. (23 Nov 2004). "Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin". Proceedings of the National Academy of Sciences of the United States of America (بالإنجليزية). 101 (47): 16588–16593. DOI:10.1073/pnas.0405496101. ISSN:0027-8424. PMC:534519. PMID:15539463. Archived from the original on 2018-11-05.

sciencedirect.com

Buskila، Dan؛ Neumann، Lily؛ Hazanov، Ilia؛ Carmi، Rivka (1 ديسمبر 1996). "Familial aggregation in the fihromyalgia syndrome". Seminars in Arthritis and Rheumatism. ج. 26 ع. 3: 605–611. DOI:10.1016/S0049-0172(96)80011-4. مؤرشف من الأصل في 2020-03-28. {{استشهاد بدورية محكمة}}: |archive-date= / |archive-url= timestamp mismatch (مساعدة)

sciencemag.org

science.sciencemag.org

Carstea, Eugene D.; Morris, Jill A.; Coleman, Katherine G.; Loftus, Stacie K.; Zhang, Dana; Cummings, Christiano; Gu, Jessie; Rosenfeld, Melissa A.; Pavan, William J. (11 Jul 1997). "Niemann-Pick C1 Disease Gene: Homology to Mediators of Cholesterol Homeostasis". Science (بالإنجليزية). 277 (5323): 228–231. DOI:10.1126/science.277.5323.228. ISSN:0036-8075. PMID:9211849. Archived from the original on 2017-12-15.

web.archive.org

Raz، Aviad E.؛ Atar، Marcela؛ Rodnay، Maya؛ Shoham-Vardi، Ilana؛ Carmi، Rivka. "Between Acculturation and Ambivalence: Knowledge of Genetics and Attitudes towards Genetic Testing in a Consanguineous Bedouin Community". Public Health Genomics. ج. 6 ع. 2: 88–95. DOI:10.1159/000073004. مؤرشف من الأصل في 2020-03-14.
Birnbaum, Ramon Y.; Landau, Daniella; Elbedour, Khalil; Ofir, Rivka; Birk, Ohad S.; Carmi, Rivka (15 Apr 2008). "Deletion of the first pair of fibronectin type III repeats of the integrin β-4 gene is associated with epidermolysis bullosa, pyloric atresia and aplasia cutis congenita in the original Carmi syndrome patients". American Journal of Medical Genetics Part A (بالإنجليزية). 146A (8): 1063–1066. DOI:10.1002/ajmg.a.31903. ISSN:1552-4833. Archived from the original on 2017-12-01.
Chiang, Annie P.; Beck, John S.; Yen, Hsan-Jan; Tayeh, Marwan K.; Scheetz, Todd E.; Swiderski, Ruth E.; Nishimura, Darryl Y.; Braun, Terry A.; Kim, Kwang-Youn A. (18 Apr 2006). "Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet–Biedl syndrome gene (BBS11)". Proceedings of the National Academy of Sciences (بالإنجليزية). 103 (16): 6287–6292. DOI:10.1073/pnas.0600158103. ISSN:0027-8424. PMC:1458870. PMID:16606853. Archived from the original on 2018-06-02.
Nishimura, Darryl Y.; Fath, Melissa; Mullins, Robert F.; Searby, Charles; Andrews, Michael; Davis, Roger; Andorf, Jeaneen L.; Mykytyn, Kirk; Swiderski, Ruth E. (23 Nov 2004). "Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin". Proceedings of the National Academy of Sciences of the United States of America (بالإنجليزية). 101 (47): 16588–16593. DOI:10.1073/pnas.0405496101. ISSN:0027-8424. PMC:534519. PMID:15539463. Archived from the original on 2018-11-05.
Mykytyn, Kirk; Nishimura, Darryl Y.; Searby, Charles C.; Shastri, Mythreyi; Yen, Hsan-jan; Beck, John S.; Braun, Terry; Streb, Luan M.; Cornier, Alberto S. (1 Aug 2002). "Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome". Nature Genetics (بالإنجليزية). 31 (4): 435–438. DOI:10.1038/ng935. ISSN:1061-4036. PMID:12118255. Archived from the original on 2006-04-11.
Walder, Roxanne Y.; Landau, Daniel; Meyer, Peter; Shalev, Hanna; Tsolia, Maria; Borochowitz, Zvi; Boettger, Melanie Barbara; Beck, Gretel E.; Englehardt, Richard K. (1 Jun 2002). "Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia". Nature Genetics (بالإنجليزية). 31 (2): 171–174. DOI:10.1038/ng901. ISSN:1061-4036. PMID:12032570. Archived from the original on 2010-10-23.
Nishimura, Darryl Y.; Searby, Charles C.; Carmi, Rivka; Elbedour, Khalil; Maldergem, Lionel Van; Fulton, Anne B.; Lam, Byron L.; Powell, Berkley R.; Swiderski, Ruth E. (2 Apr 2001). "Positional cloning of a novel gene on chromosome 16q causing Bardet–Biedl syndrome (BBS2)". Human Molecular Genetics (بالإنجليزية). 10 (8): 865–874. DOI:10.1093/hmg/10.8.865. ISSN:0964-6906. PMID:11285252. Archived from the original on 2016-05-17.
Haider, Neena B.; Jacobson, Samuel G.; Cideciyan, Artur V.; Swiderski, Ruth; Streb, Luan M.; Searby, Charles; Beck, Gretel; Hockey, Robin; Hanna, David B. (1 Feb 2000). "Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate". Nature Genetics (بالإنجليزية). 24 (2): 127–131. DOI:10.1038/72777. ISSN:1061-4036. PMID:10655056. Archived from the original on 2016-11-05.
Carstea, Eugene D.; Morris, Jill A.; Coleman, Katherine G.; Loftus, Stacie K.; Zhang, Dana; Cummings, Christiano; Gu, Jessie; Rosenfeld, Melissa A.; Pavan, William J. (11 Jul 1997). "Niemann-Pick C1 Disease Gene: Homology to Mediators of Cholesterol Homeostasis". Science (بالإنجليزية). 277 (5323): 228–231. DOI:10.1126/science.277.5323.228. ISSN:0036-8075. PMID:9211849. Archived from the original on 2017-12-15.
Maman, Eran; Maor, Esther; Kachko, Leonid; Carmi, Rivka (30 Jun 1998). "Epidermolysis bullosa, pyloric atresia, aplasia cutis congenita: Histopathological delineation of an autosomal recessive disease". American Journal of Medical Genetics (بالإنجليزية). 78 (2): 127–133. DOI:10.1002/(sici)1096-8628(19980630)78:2<127::aid-ajmg6>3.0.co;2-l. ISSN:1096-8628. Archived from the original on 2023-11-17.
Scott, Da; Kraft, Ml; Carmi, R; Ramesh, A; Elbedour, K; Yairi, Y; Srisailapathy, C. R. Srikumari; Rosengren, Ss; Markham, Af (1 Jan 1998). "Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss". Human Mutation (بالإنجليزية). 11 (5): 387–394. DOI:10.1002/(sici)1098-1004(1998)11:5<387::aid-humu6>3.0.co;2-8. ISSN:1098-1004. Archived from the original on 2022-05-17.
Buskila، Dan؛ Neumann، Lily؛ Hazanov، Ilia؛ Carmi، Rivka (1 ديسمبر 1996). "Familial aggregation in the fihromyalgia syndrome". Seminars in Arthritis and Rheumatism. ج. 26 ع. 3: 605–611. DOI:10.1016/S0049-0172(96)80011-4. مؤرشف من الأصل في 2020-03-28. {{استشهاد بدورية محكمة}}: |archive-date= / |archive-url= timestamp mismatch (مساعدة)
Sheffield, Val C.; Carml, Rivka; Kwltek-Black, Anne; Rokhlina, Tatiana; Nishlmura, Darryl; Duyk, Geoffrey M.; Elbedour, Khalil; Sunden, Sara L.; Stone, Edwin M. (1 Aug 1994). "Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping". Human Molecular Genetics (بالإنجليزية). 3 (8): 1331–1335. DOI:10.1093/hmg/3.8.1331. ISSN:0964-6906. PMID:7987310. Archived from the original on 2020-04-14.
Carmi, R.; Gohar, J.; Meizner, I.; Katz, M. (1 Jun 1994). "Spontaneous abortion–high risk factor for neural tube defects in subsequent pregnancy". American Journal of Medical Genetics (بالإنجليزية). 51 (2): 93–97. DOI:10.1002/ajmg.1320510203. ISSN:1096-8628. Archived from the original on 2017-12-01.
Parvari, R.; Weinstein, Y.; Ehrlich, S.; Steinitz, M.; Carmi, R. (15 Feb 1994). "Linkage localization of the thoraco-abdominal syndrome (TAS) gene to Xq25–26". American Journal of Medical Genetics (بالإنجليزية). 49 (4): 431–434. DOI:10.1002/ajmg.1320490416. ISSN:1096-8628. PMID:7909197. Archived from the original on 2018-02-17.
Kwitek-Black, Anne E.; Carmi, Rivka; Duyk, Geoffrey M.; Buetow, Kenneth H.; Elbedour, Khalil; Parvari, Ruti; Yandava, Chandra Naidu; Stone, Edwin M.; Sheffield, Val C. (1 Dec 1993). "Linkage of Bardet–Biedl syndrome to chromosome 16q and evidence for non–allelic genetic heterogeneity". Nature Genetics (بالإنجليزية). 5 (4): 392–396. DOI:10.1038/ng1293-392. PMID:8298649. Archived from the original on 2015-01-28.
Carmi, Rivka; Boughman, Joann A. (1 Jan 1992). "Pentalogy of Cantrell and associated midline anomalies: A possible ventral midline developmental field". American Journal of Medical Genetics (بالإنجليزية). 42 (1): 90–95. DOI:10.1002/ajmg.1320420118. ISSN:1096-8628. PMID:1308371. Archived from the original on 2017-12-01.
Carmi, R.; Meizner, I.; Katz, M. (1 Jul 1990). "Familial congenital diaphragmatic defect and associated midline anomalies: Further evidence for an X-linked midline gene?". American Journal of Medical Genetics (بالإنجليزية). 36 (3): 313–315. DOI:10.1002/ajmg.1320360314. ISSN:1096-8628. PMID:2363430. Archived from the original on 2018-02-17.
Carmi, R.; Sofer, S.; Karplus, M.; Ben-Yakar, Y.; Mahler, D.; Zirkin, H.; Bar-Ziv, J.; Opitz, John M. (1 Mar 1982). "Aplasia cutis congenita in two sibs discordant for pylori atresia". American Journal of Medical Genetics (بالإنجليزية). 11 (3): 319–328. DOI:10.1002/ajmg.1320110308. ISSN:1096-8628. Archived from the original on 2017-12-01.
"OMIM - % 313850 - THORACOABDOMINAL SYNDROME; THAS". www.omim.org. مؤرشف من الأصل في 2019-04-25. اطلع عليه بتاريخ 2016-09-08.
"OMIM Entry - # 226730 - CARMI SYNDROME". www.omim.org. مؤرشف من الأصل في 2020-01-09. اطلع عليه بتاريخ 2016-09-08.
Carmi, R.; Barbash, A.; Mares, A. J. (1 May 1990). "The thoracoabdominal syndrome (TAS): A new X-linked dominant disorder". American Journal of Medical Genetics (بالإنجليزية). 36 (1): 109–114. DOI:10.1002/ajmg.1320360122. ISSN:1096-8628. PMID:2139758. Archived from the original on 2017-12-01.
צור، ירדן (22 نوفمبر 2017). "חרף ההנחיות, אונ' בן גוריון רוצה להאריך את כהונת הנשיאה; הפרופסורים מתנגדים". הארץ (بالعبرية). مؤرشف من الأصل في 2017-12-01. اطلع عليه بتاريخ 2017-11-26.
צור، ירדן (21 ديسمبر 2017). "מחריף המשבר באונ' בן גוריון: נעצר הליך מינוי הרקטור החדש". הארץ (بالعبرية). مؤرشف من الأصل في 2018-02-07. اطلع عليه بتاريخ 2018-02-06.
"מבקר המדינה בודק הארכת מינויה של נשיאת אוניברסיטת בן גוריון". ערוץ עשר (بالعبرية). مؤرشف من الأصل في 2018-02-07. اطلع عليه بتاريخ 2018-02-06.
(Tzur) צור، (Yarden) ירדן (2 يناير 2018). "(The president of Ben-Gurion University responds to the protest) נשיא אוניברסיטת בן גוריון מגיב למחאה". הארץ (بالعبرية). Ha'aretz. مؤرشف من الأصل في 2018-01-21. اطلع عليه بتاريخ 2018-01-21.
צור، ירדן (5 فبراير 2018). "אוניברסיטת בן גוריון: נבחר נשיא חדש עד תום 2018". הארץ (بالعبرية). مؤرشف من الأصل في 2018-05-08. اطلع عليه بتاريخ 2018-02-06.

wiley.com

onlinelibrary.wiley.com

Birnbaum, Ramon Y.; Landau, Daniella; Elbedour, Khalil; Ofir, Rivka; Birk, Ohad S.; Carmi, Rivka (15 Apr 2008). "Deletion of the first pair of fibronectin type III repeats of the integrin β-4 gene is associated with epidermolysis bullosa, pyloric atresia and aplasia cutis congenita in the original Carmi syndrome patients". American Journal of Medical Genetics Part A (بالإنجليزية). 146A (8): 1063–1066. DOI:10.1002/ajmg.a.31903. ISSN:1552-4833. Archived from the original on 2017-12-01.
Maman, Eran; Maor, Esther; Kachko, Leonid; Carmi, Rivka (30 Jun 1998). "Epidermolysis bullosa, pyloric atresia, aplasia cutis congenita: Histopathological delineation of an autosomal recessive disease". American Journal of Medical Genetics (بالإنجليزية). 78 (2): 127–133. DOI:10.1002/(sici)1096-8628(19980630)78:2<127::aid-ajmg6>3.0.co;2-l. ISSN:1096-8628. Archived from the original on 2023-11-17.
Scott, Da; Kraft, Ml; Carmi, R; Ramesh, A; Elbedour, K; Yairi, Y; Srisailapathy, C. R. Srikumari; Rosengren, Ss; Markham, Af (1 Jan 1998). "Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss". Human Mutation (بالإنجليزية). 11 (5): 387–394. DOI:10.1002/(sici)1098-1004(1998)11:5<387::aid-humu6>3.0.co;2-8. ISSN:1098-1004. Archived from the original on 2022-05-17.
Carmi, R.; Gohar, J.; Meizner, I.; Katz, M. (1 Jun 1994). "Spontaneous abortion–high risk factor for neural tube defects in subsequent pregnancy". American Journal of Medical Genetics (بالإنجليزية). 51 (2): 93–97. DOI:10.1002/ajmg.1320510203. ISSN:1096-8628. Archived from the original on 2017-12-01.
Parvari, R.; Weinstein, Y.; Ehrlich, S.; Steinitz, M.; Carmi, R. (15 Feb 1994). "Linkage localization of the thoraco-abdominal syndrome (TAS) gene to Xq25–26". American Journal of Medical Genetics (بالإنجليزية). 49 (4): 431–434. DOI:10.1002/ajmg.1320490416. ISSN:1096-8628. PMID:7909197. Archived from the original on 2018-02-17.
Carmi, Rivka; Boughman, Joann A. (1 Jan 1992). "Pentalogy of Cantrell and associated midline anomalies: A possible ventral midline developmental field". American Journal of Medical Genetics (بالإنجليزية). 42 (1): 90–95. DOI:10.1002/ajmg.1320420118. ISSN:1096-8628. PMID:1308371. Archived from the original on 2017-12-01.
Carmi, R.; Meizner, I.; Katz, M. (1 Jul 1990). "Familial congenital diaphragmatic defect and associated midline anomalies: Further evidence for an X-linked midline gene?". American Journal of Medical Genetics (بالإنجليزية). 36 (3): 313–315. DOI:10.1002/ajmg.1320360314. ISSN:1096-8628. PMID:2363430. Archived from the original on 2018-02-17.
Carmi, R.; Sofer, S.; Karplus, M.; Ben-Yakar, Y.; Mahler, D.; Zirkin, H.; Bar-Ziv, J.; Opitz, John M. (1 Mar 1982). "Aplasia cutis congenita in two sibs discordant for pylori atresia". American Journal of Medical Genetics (بالإنجليزية). 11 (3): 319–328. DOI:10.1002/ajmg.1320110308. ISSN:1096-8628. Archived from the original on 2017-12-01.
Carmi, R.; Barbash, A.; Mares, A. J. (1 May 1990). "The thoracoabdominal syndrome (TAS): A new X-linked dominant disorder". American Journal of Medical Genetics (بالإنجليزية). 36 (1): 109–114. DOI:10.1002/ajmg.1320360122. ISSN:1096-8628. PMID:2139758. Archived from the original on 2017-12-01.

worldcat.org

Scott، D. A.؛ Carmi، R.؛ Elbedour، K.؛ Yosefsberg، S.؛ Stone، E. M.؛ Sheffield، V. C. (1 أغسطس 1996). "An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindreds". American Journal of Human Genetics. ج. 59 ع. 2: 385–391. ISSN:0002-9297. PMC:1914732. PMID:8755925.
Scott، D. A.؛ Carmi، R.؛ Elbedour، K.؛ Duyk، G. M.؛ Stone، E. M.؛ Sheffield، V. C. (1 أكتوبر 1995). "Nonsyndromic autosomal recessive deafness is linked to the DFNB1 locus in a large inbred Bedouin family from Israel". American Journal of Human Genetics. ج. 57 ع. 4: 965–968. ISSN:0002-9297. PMC:1801487. PMID:7573061.
Birnbaum, Ramon Y.; Landau, Daniella; Elbedour, Khalil; Ofir, Rivka; Birk, Ohad S.; Carmi, Rivka (15 Apr 2008). "Deletion of the first pair of fibronectin type III repeats of the integrin β-4 gene is associated with epidermolysis bullosa, pyloric atresia and aplasia cutis congenita in the original Carmi syndrome patients". American Journal of Medical Genetics Part A (بالإنجليزية). 146A (8): 1063–1066. DOI:10.1002/ajmg.a.31903. ISSN:1552-4833. Archived from the original on 2017-12-01.
Chiang, Annie P.; Beck, John S.; Yen, Hsan-Jan; Tayeh, Marwan K.; Scheetz, Todd E.; Swiderski, Ruth E.; Nishimura, Darryl Y.; Braun, Terry A.; Kim, Kwang-Youn A. (18 Apr 2006). "Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet–Biedl syndrome gene (BBS11)". Proceedings of the National Academy of Sciences (بالإنجليزية). 103 (16): 6287–6292. DOI:10.1073/pnas.0600158103. ISSN:0027-8424. PMC:1458870. PMID:16606853. Archived from the original on 2018-06-02.
Nishimura, Darryl Y.; Fath, Melissa; Mullins, Robert F.; Searby, Charles; Andrews, Michael; Davis, Roger; Andorf, Jeaneen L.; Mykytyn, Kirk; Swiderski, Ruth E. (23 Nov 2004). "Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin". Proceedings of the National Academy of Sciences of the United States of America (بالإنجليزية). 101 (47): 16588–16593. DOI:10.1073/pnas.0405496101. ISSN:0027-8424. PMC:534519. PMID:15539463. Archived from the original on 2018-11-05.
Mykytyn, Kirk; Nishimura, Darryl Y.; Searby, Charles C.; Shastri, Mythreyi; Yen, Hsan-jan; Beck, John S.; Braun, Terry; Streb, Luan M.; Cornier, Alberto S. (1 Aug 2002). "Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome". Nature Genetics (بالإنجليزية). 31 (4): 435–438. DOI:10.1038/ng935. ISSN:1061-4036. PMID:12118255. Archived from the original on 2006-04-11.
Walder, Roxanne Y.; Landau, Daniel; Meyer, Peter; Shalev, Hanna; Tsolia, Maria; Borochowitz, Zvi; Boettger, Melanie Barbara; Beck, Gretel E.; Englehardt, Richard K. (1 Jun 2002). "Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia". Nature Genetics (بالإنجليزية). 31 (2): 171–174. DOI:10.1038/ng901. ISSN:1061-4036. PMID:12032570. Archived from the original on 2010-10-23.
Nishimura, Darryl Y.; Searby, Charles C.; Carmi, Rivka; Elbedour, Khalil; Maldergem, Lionel Van; Fulton, Anne B.; Lam, Byron L.; Powell, Berkley R.; Swiderski, Ruth E. (2 Apr 2001). "Positional cloning of a novel gene on chromosome 16q causing Bardet–Biedl syndrome (BBS2)". Human Molecular Genetics (بالإنجليزية). 10 (8): 865–874. DOI:10.1093/hmg/10.8.865. ISSN:0964-6906. PMID:11285252. Archived from the original on 2016-05-17.
Haider, Neena B.; Jacobson, Samuel G.; Cideciyan, Artur V.; Swiderski, Ruth; Streb, Luan M.; Searby, Charles; Beck, Gretel; Hockey, Robin; Hanna, David B. (1 Feb 2000). "Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate". Nature Genetics (بالإنجليزية). 24 (2): 127–131. DOI:10.1038/72777. ISSN:1061-4036. PMID:10655056. Archived from the original on 2016-11-05.
Carstea, Eugene D.; Morris, Jill A.; Coleman, Katherine G.; Loftus, Stacie K.; Zhang, Dana; Cummings, Christiano; Gu, Jessie; Rosenfeld, Melissa A.; Pavan, William J. (11 Jul 1997). "Niemann-Pick C1 Disease Gene: Homology to Mediators of Cholesterol Homeostasis". Science (بالإنجليزية). 277 (5323): 228–231. DOI:10.1126/science.277.5323.228. ISSN:0036-8075. PMID:9211849. Archived from the original on 2017-12-15.
Maman, Eran; Maor, Esther; Kachko, Leonid; Carmi, Rivka (30 Jun 1998). "Epidermolysis bullosa, pyloric atresia, aplasia cutis congenita: Histopathological delineation of an autosomal recessive disease". American Journal of Medical Genetics (بالإنجليزية). 78 (2): 127–133. DOI:10.1002/(sici)1096-8628(19980630)78:2<127::aid-ajmg6>3.0.co;2-l. ISSN:1096-8628. Archived from the original on 2023-11-17.
Scott, Da; Kraft, Ml; Carmi, R; Ramesh, A; Elbedour, K; Yairi, Y; Srisailapathy, C. R. Srikumari; Rosengren, Ss; Markham, Af (1 Jan 1998). "Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss". Human Mutation (بالإنجليزية). 11 (5): 387–394. DOI:10.1002/(sici)1098-1004(1998)11:5<387::aid-humu6>3.0.co;2-8. ISSN:1098-1004. Archived from the original on 2022-05-17.
Carmi، R.؛ Rokhlina، T.؛ Kwitek-Black، A. E.؛ Elbedour، K.؛ Nishimura، D.؛ Stone، E. M.؛ Sheffield، V. C. (1 يناير 1995). "Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15". Human Molecular Genetics. ج. 4 ع. 1: 9–13. DOI:10.1093/hmg/4.1.9. ISSN:0964-6906. PMID:7711739.
Sheffield, Val C.; Carml, Rivka; Kwltek-Black, Anne; Rokhlina, Tatiana; Nishlmura, Darryl; Duyk, Geoffrey M.; Elbedour, Khalil; Sunden, Sara L.; Stone, Edwin M. (1 Aug 1994). "Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping". Human Molecular Genetics (بالإنجليزية). 3 (8): 1331–1335. DOI:10.1093/hmg/3.8.1331. ISSN:0964-6906. PMID:7987310. Archived from the original on 2020-04-14.
Carmi, R.; Gohar, J.; Meizner, I.; Katz, M. (1 Jun 1994). "Spontaneous abortion–high risk factor for neural tube defects in subsequent pregnancy". American Journal of Medical Genetics (بالإنجليزية). 51 (2): 93–97. DOI:10.1002/ajmg.1320510203. ISSN:1096-8628. Archived from the original on 2017-12-01.
Parvari, R.; Weinstein, Y.; Ehrlich, S.; Steinitz, M.; Carmi, R. (15 Feb 1994). "Linkage localization of the thoraco-abdominal syndrome (TAS) gene to Xq25–26". American Journal of Medical Genetics (بالإنجليزية). 49 (4): 431–434. DOI:10.1002/ajmg.1320490416. ISSN:1096-8628. PMID:7909197. Archived from the original on 2018-02-17.
Carmi, Rivka; Boughman, Joann A. (1 Jan 1992). "Pentalogy of Cantrell and associated midline anomalies: A possible ventral midline developmental field". American Journal of Medical Genetics (بالإنجليزية). 42 (1): 90–95. DOI:10.1002/ajmg.1320420118. ISSN:1096-8628. PMID:1308371. Archived from the original on 2017-12-01.
Carmi, R.; Meizner, I.; Katz, M. (1 Jul 1990). "Familial congenital diaphragmatic defect and associated midline anomalies: Further evidence for an X-linked midline gene?". American Journal of Medical Genetics (بالإنجليزية). 36 (3): 313–315. DOI:10.1002/ajmg.1320360314. ISSN:1096-8628. PMID:2363430. Archived from the original on 2018-02-17.
Carmi, R.; Sofer, S.; Karplus, M.; Ben-Yakar, Y.; Mahler, D.; Zirkin, H.; Bar-Ziv, J.; Opitz, John M. (1 Mar 1982). "Aplasia cutis congenita in two sibs discordant for pylori atresia". American Journal of Medical Genetics (بالإنجليزية). 11 (3): 319–328. DOI:10.1002/ajmg.1320110308. ISSN:1096-8628. Archived from the original on 2017-12-01.
Carmi, R.; Barbash, A.; Mares, A. J. (1 May 1990). "The thoracoabdominal syndrome (TAS): A new X-linked dominant disorder". American Journal of Medical Genetics (بالإنجليزية). 36 (1): 109–114. DOI:10.1002/ajmg.1320360122. ISSN:1096-8628. PMID:2139758. Archived from the original on 2017-12-01.