متلازمة ذكر إكس إكس (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "متلازمة ذكر إكس إكس" in Arabic language version.

refsWebsite

Global rank Arabic rank

17doi.org

2^nd place

5^th place

15issn.org

57^th place

1,629^th place

13web.archive.org

1^st place

11nih.gov

4^th place

6^th place

4oup.com

485^th place

407^th place

2bmj.com

1,226^th place

531^st place

2wiley.com

222^nd place

221^st place

1archive.org

6^th place

3^rd place

1sciencedirect.com

149^th place

233^rd place

1nature.com

234^th place

251^st place

1scielo.br

1,606^th place

3,279^th place

1omim.org

4,380^th place

2,257^th place

1fertstert.org

low place

archive.org (Global: 6^th place; Arabic: 3^rd place)

de la Chapelle، A (يناير 1972). "Analytic review: nature and origin of males with XX sex chromosomes". American Journal of Human Genetics. ج. 24 ع. 1: 71–105. ISSN:0002-9297. PMC:1762158. PMID:4622299.

bmj.com (Global: 1,226^th place; Arabic: 531^st place)

jmg.bmj.com

Kusz, Kamila; Kotecki, Maciej; Wojda, Alina; Szarras-Czapnik, Maria; Latos-Bielenska, Anna; Warenik-Szymankiewicz, Alina; Ruszczynska-Wolska, Anna; Jaruzelska, Jadwiga (1 Jun 1999). "Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome". Journal of Medical Genetics (بالإنجليزية). 36 (6): 452–456. DOI:10.1136/jmg.36.6.452. ISSN:0022-2593. PMC:1734388. PMID:10874632. Archived from the original on 2019-03-30.
Vetro, Annalisa; Ciccone, Roberto; Giorda, Roberto; Patricelli, Maria Grazia; Mina, Erika Della; Forlino, Antonella; Zuffardi, Orsetta (1 Jan 2011). "XX males SRY negative: a confirmed cause of infertility". Journal of Medical Genetics (بالإنجليزية). 48: jmedgenet–2011–100036. DOI:10.1136/jmedgenet-2011-100036. ISSN:0022-2593. PMC:3178810. PMID:21653197. Archived from the original on 2017-12-01.

doi.org (Global: 2^nd place; Arabic: 5^th place)

Vorona، Elena؛ Zitzmann، Michael؛ Gromoll، Jörg؛ Schüring، Andreas N.؛ Nieschlag، Eberhard (1 سبتمبر 2007). "Clinical, Endocrinological, and Epigenetic Features of the 46,XX Male Syndrome, Compared with 47,XXY Klinefelter Patients". The Journal of Clinical Endocrinology & Metabolism. ج. 92 ع. 9: 3458–3465. DOI:10.1210/jc.2007-0447. ISSN:0021-972X. مؤرشف من الأصل في 2018-07-04.
Anık، Ahmet؛ Çatlı، Gönül؛ Abacı، Ayhan؛ Böber، Ece (2013). "46,XX Male Disorder of Sexual Development: A Case Report". Journal of Clinical Research in Pediatric Endocrinology. ج. 5 ع. 4: 258–260. DOI:10.4274/Jcrpe.1098. ISSN:1308-5727. PMC:3890225. PMID:24379036.
Ucan، Bekir؛ Ozbek، Mustafa؛ Topaloglu، Oya؛ Yesilurt، Ahmet؛ Gungunes، Askin؛ Demrici، Taner؛ Delibasi، Tunfay (يوليو 2012). "46,XX Male Syndrome". Turkish Journal of Endocrinology and Metabolism. ج. 17: 46–48. DOI:10.4274/Tjem.2064.
Chen، Harold (2012). "XX Male". Atlas of Genetic Diagnosis and Counseling: 2191–2196. DOI:10.1007/978-1-4614-1037-9_250.
Vorona, Elena; Zitzmann, Michael; Gromoll, Jörg; Schüring, Andreas N.; Nieschlag, Eberhard (1 Sep 2007). "Clinical, Endocrinological, and Epigenetic Features of the 46,XX Male Syndrome, Compared with 47,XXY Klinefelter Patients". The Journal of Clinical Endocrinology & Metabolism (بالإنجليزية). 92 (9): 3458–3465. DOI:10.1210/jc.2007-0447. ISSN:0021-972X. Archived from the original on 2018-07-04.
Lisker، R؛ Flores، F؛ Cobo، A؛ Rojas، F G (ديسمبر 1970). "A case of XX male syndrome". Journal of Medical Genetics. ج. 7 ع. 4: 394–398. DOI:10.1136/jmg.7.4.394. ISSN:0022-2593. PMC:1468937. PMID:5501706.
Abusheikha, N.; Lass, A.; Brinsden, P. (1 Apr 2001). "XX males without SRY gene and with infertility: Case report". Human Reproduction (بالإنجليزية). 16 (4): 717–718. DOI:10.1093/humrep/16.4.717. ISSN:0268-1161. Archived from the original on 2018-07-07.
Kusz, Kamila; Kotecki, Maciej; Wojda, Alina; Szarras-Czapnik, Maria; Latos-Bielenska, Anna; Warenik-Szymankiewicz, Alina; Ruszczynska-Wolska, Anna; Jaruzelska, Jadwiga (1 Jun 1999). "Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome". Journal of Medical Genetics (بالإنجليزية). 36 (6): 452–456. DOI:10.1136/jmg.36.6.452. ISSN:0022-2593. PMC:1734388. PMID:10874632. Archived from the original on 2019-03-30.
Bouayed Abdelmoula، Nouha؛ Portnoi، Marie-France؛ Keskes، Leila؛ Recan، Dominique؛ Bahloul، Ali؛ Boudawara، Tahia؛ Saad، Ali؛ Rebai، Tarek (1 يناير 2003). "Skewed X-chromosome inactivation pattern in SRY positive XX maleness: a case report and review of literature". Annales de Génétique. ج. 46 ع. 1: 11–18. DOI:10.1016/S0003-3995(03)00011-X. مؤرشف من الأصل في 2019-12-13.
Margarit, Ester; Coll, M. Dolors; Oliva, Rafael; Gómez, David; Soler, Anna; Ballesta, Francisca (3 Jan 2000). "SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphrodite". American Journal of Medical Genetics (بالإنجليزية). 90 (1): 25–28. DOI:10.1002/(sici)1096-8628(20000103)90:1<25::aid-ajmg5>3.0.co;2-5. ISSN:1096-8628. Archived from the original on 2023-04-19.
Vetro, Annalisa; Ciccone, Roberto; Giorda, Roberto; Patricelli, Maria Grazia; Mina, Erika Della; Forlino, Antonella; Zuffardi, Orsetta (1 Jan 2011). "XX males SRY negative: a confirmed cause of infertility". Journal of Medical Genetics (بالإنجليزية). 48: jmedgenet–2011–100036. DOI:10.1136/jmedgenet-2011-100036. ISSN:0022-2593. PMC:3178810. PMID:21653197. Archived from the original on 2017-12-01.
Rajender, S. (1 May 2006). "SRY-negative 46,XX male with normal genitals, complete masculinization and infertility". Molecular Human Reproduction (بالإنجليزية). 12 (5): 341–346. DOI:10.1093/molehr/gal030. ISSN:1360-9947. Archived from the original on 2019-02-24.
Swain, Amanda; Narvaez, Veronica; Burgoyne, Paul; Camerino, Giovanna; Lovell-Badge, Robin (19 Feb 1998). "Dax1 antagonizes Sry action in mammalian sex determination". Nature (بالإنجليزية). 391 (6669): 761–767. DOI:10.1038/35799. ISSN:1476-4687. Archived from the original on 2019-12-13.
Domenice، S.؛ Corrêa، R. V.؛ Costa، E. M. F.؛ Nishi، M. Y.؛ Vilain، E.؛ Arnhold، I. J. P.؛ Mendonca، B. B. (يناير 2004). "Mutations in the SRY, DAX1, SF1 and WNT4 genes in Brazilian sex-reversed patients". Brazilian Journal of Medical and Biological Research. ج. 37 ع. 1: 145–150. DOI:10.1590/S0100-879X2004000100020. ISSN:0100-879X. مؤرشف من الأصل في 2010-12-20.
Aksglaede, L.; Jørgensen, N.; Skakkebæk, N. E.; Juul, A. (1 Aug 2009). "Low semen volume in 47 adolescents and adults with 47,XXY Klinefelter or 46,XX male syndrome". International Journal of Andrology (بالإنجليزية). 32 (4): 376–384. DOI:10.1111/j.1365-2605.2008.00921.x. ISSN:1365-2605. Archived from the original on 2017-12-01.
Parada-Bustamante, Alexis; Ríos, Rafael; Ebensperger, Mauricio; Lardone, María Cecilia; Piottante, Antonio; Castro, Andrea (1 Nov 2010). "46,XX/SRY-negative true hermaphrodite". Fertility and Sterility (بالإنجليزية). 94 (6): 2330.e13–2330.e16. DOI:10.1016/j.fertnstert.2010.03.066. ISSN:0015-0282. Archived from the original on 2019-12-13.
Kurita، Masakazu؛ Aiba، Emiko؛ Matsumoto، Daisuke؛ Sato، Katsujiro؛ Nagase، Takashi؛ Yoshimura، Kotaro (مايو 2006). "Feminizing genitoplasty for treatment of XX male with masculine genitalia". Plastic and Reconstructive Surgery. ج. 117 ع. 6: 107e–111e. DOI:10.1097/01.prs.0000214653.30135.a1. ISSN:1529-4242. PMID:16651931.

fertstert.org (Global: low place; Arabic: low place)

Parada-Bustamante, Alexis; Ríos, Rafael; Ebensperger, Mauricio; Lardone, María Cecilia; Piottante, Antonio; Castro, Andrea (1 Nov 2010). "46,XX/SRY-negative true hermaphrodite". Fertility and Sterility (بالإنجليزية). 94 (6): 2330.e13–2330.e16. DOI:10.1016/j.fertnstert.2010.03.066. ISSN:0015-0282. Archived from the original on 2019-12-13.

issn.org (Global: 57^th place; Arabic: 1,629^th place)

portal.issn.org

de la Chapelle، A (يناير 1972). "Analytic review: nature and origin of males with XX sex chromosomes". American Journal of Human Genetics. ج. 24 ع. 1: 71–105. ISSN:0002-9297. PMC:1762158. PMID:4622299.
Vorona، Elena؛ Zitzmann، Michael؛ Gromoll، Jörg؛ Schüring، Andreas N.؛ Nieschlag، Eberhard (1 سبتمبر 2007). "Clinical, Endocrinological, and Epigenetic Features of the 46,XX Male Syndrome, Compared with 47,XXY Klinefelter Patients". The Journal of Clinical Endocrinology & Metabolism. ج. 92 ع. 9: 3458–3465. DOI:10.1210/jc.2007-0447. ISSN:0021-972X. مؤرشف من الأصل في 2018-07-04.
Anık، Ahmet؛ Çatlı، Gönül؛ Abacı، Ayhan؛ Böber، Ece (2013). "46,XX Male Disorder of Sexual Development: A Case Report". Journal of Clinical Research in Pediatric Endocrinology. ج. 5 ع. 4: 258–260. DOI:10.4274/Jcrpe.1098. ISSN:1308-5727. PMC:3890225. PMID:24379036.
Vorona, Elena; Zitzmann, Michael; Gromoll, Jörg; Schüring, Andreas N.; Nieschlag, Eberhard (1 Sep 2007). "Clinical, Endocrinological, and Epigenetic Features of the 46,XX Male Syndrome, Compared with 47,XXY Klinefelter Patients". The Journal of Clinical Endocrinology & Metabolism (بالإنجليزية). 92 (9): 3458–3465. DOI:10.1210/jc.2007-0447. ISSN:0021-972X. Archived from the original on 2018-07-04.
Lisker، R؛ Flores، F؛ Cobo، A؛ Rojas، F G (ديسمبر 1970). "A case of XX male syndrome". Journal of Medical Genetics. ج. 7 ع. 4: 394–398. DOI:10.1136/jmg.7.4.394. ISSN:0022-2593. PMC:1468937. PMID:5501706.
Abusheikha, N.; Lass, A.; Brinsden, P. (1 Apr 2001). "XX males without SRY gene and with infertility: Case report". Human Reproduction (بالإنجليزية). 16 (4): 717–718. DOI:10.1093/humrep/16.4.717. ISSN:0268-1161. Archived from the original on 2018-07-07.
Kusz, Kamila; Kotecki, Maciej; Wojda, Alina; Szarras-Czapnik, Maria; Latos-Bielenska, Anna; Warenik-Szymankiewicz, Alina; Ruszczynska-Wolska, Anna; Jaruzelska, Jadwiga (1 Jun 1999). "Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome". Journal of Medical Genetics (بالإنجليزية). 36 (6): 452–456. DOI:10.1136/jmg.36.6.452. ISSN:0022-2593. PMC:1734388. PMID:10874632. Archived from the original on 2019-03-30.
Margarit, Ester; Coll, M. Dolors; Oliva, Rafael; Gómez, David; Soler, Anna; Ballesta, Francisca (3 Jan 2000). "SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphrodite". American Journal of Medical Genetics (بالإنجليزية). 90 (1): 25–28. DOI:10.1002/(sici)1096-8628(20000103)90:1<25::aid-ajmg5>3.0.co;2-5. ISSN:1096-8628. Archived from the original on 2023-04-19.
Vetro, Annalisa; Ciccone, Roberto; Giorda, Roberto; Patricelli, Maria Grazia; Mina, Erika Della; Forlino, Antonella; Zuffardi, Orsetta (1 Jan 2011). "XX males SRY negative: a confirmed cause of infertility". Journal of Medical Genetics (بالإنجليزية). 48: jmedgenet–2011–100036. DOI:10.1136/jmedgenet-2011-100036. ISSN:0022-2593. PMC:3178810. PMID:21653197. Archived from the original on 2017-12-01.
Rajender, S. (1 May 2006). "SRY-negative 46,XX male with normal genitals, complete masculinization and infertility". Molecular Human Reproduction (بالإنجليزية). 12 (5): 341–346. DOI:10.1093/molehr/gal030. ISSN:1360-9947. Archived from the original on 2019-02-24.
Swain, Amanda; Narvaez, Veronica; Burgoyne, Paul; Camerino, Giovanna; Lovell-Badge, Robin (19 Feb 1998). "Dax1 antagonizes Sry action in mammalian sex determination". Nature (بالإنجليزية). 391 (6669): 761–767. DOI:10.1038/35799. ISSN:1476-4687. Archived from the original on 2019-12-13.
Domenice، S.؛ Corrêa، R. V.؛ Costa، E. M. F.؛ Nishi، M. Y.؛ Vilain، E.؛ Arnhold، I. J. P.؛ Mendonca، B. B. (يناير 2004). "Mutations in the SRY, DAX1, SF1 and WNT4 genes in Brazilian sex-reversed patients". Brazilian Journal of Medical and Biological Research. ج. 37 ع. 1: 145–150. DOI:10.1590/S0100-879X2004000100020. ISSN:0100-879X. مؤرشف من الأصل في 2010-12-20.
Aksglaede, L.; Jørgensen, N.; Skakkebæk, N. E.; Juul, A. (1 Aug 2009). "Low semen volume in 47 adolescents and adults with 47,XXY Klinefelter or 46,XX male syndrome". International Journal of Andrology (بالإنجليزية). 32 (4): 376–384. DOI:10.1111/j.1365-2605.2008.00921.x. ISSN:1365-2605. Archived from the original on 2017-12-01.
Parada-Bustamante, Alexis; Ríos, Rafael; Ebensperger, Mauricio; Lardone, María Cecilia; Piottante, Antonio; Castro, Andrea (1 Nov 2010). "46,XX/SRY-negative true hermaphrodite". Fertility and Sterility (بالإنجليزية). 94 (6): 2330.e13–2330.e16. DOI:10.1016/j.fertnstert.2010.03.066. ISSN:0015-0282. Archived from the original on 2019-12-13.
Kurita، Masakazu؛ Aiba، Emiko؛ Matsumoto، Daisuke؛ Sato، Katsujiro؛ Nagase، Takashi؛ Yoshimura، Kotaro (مايو 2006). "Feminizing genitoplasty for treatment of XX male with masculine genitalia". Plastic and Reconstructive Surgery. ج. 117 ع. 6: 107e–111e. DOI:10.1097/01.prs.0000214653.30135.a1. ISSN:1529-4242. PMID:16651931.

nature.com (Global: 234^th place; Arabic: 251^st place)

Swain, Amanda; Narvaez, Veronica; Burgoyne, Paul; Camerino, Giovanna; Lovell-Badge, Robin (19 Feb 1998). "Dax1 antagonizes Sry action in mammalian sex determination". Nature (بالإنجليزية). 391 (6669): 761–767. DOI:10.1038/35799. ISSN:1476-4687. Archived from the original on 2019-12-13.

nih.gov (Global: 4^th place; Arabic: 6^th place)

pubmed.ncbi.nlm.nih.gov

de la Chapelle، A (يناير 1972). "Analytic review: nature and origin of males with XX sex chromosomes". American Journal of Human Genetics. ج. 24 ع. 1: 71–105. ISSN:0002-9297. PMC:1762158. PMID:4622299.
Anık، Ahmet؛ Çatlı، Gönül؛ Abacı، Ayhan؛ Böber، Ece (2013). "46,XX Male Disorder of Sexual Development: A Case Report". Journal of Clinical Research in Pediatric Endocrinology. ج. 5 ع. 4: 258–260. DOI:10.4274/Jcrpe.1098. ISSN:1308-5727. PMC:3890225. PMID:24379036.
Lisker، R؛ Flores، F؛ Cobo، A؛ Rojas، F G (ديسمبر 1970). "A case of XX male syndrome". Journal of Medical Genetics. ج. 7 ع. 4: 394–398. DOI:10.1136/jmg.7.4.394. ISSN:0022-2593. PMC:1468937. PMID:5501706.
Kusz, Kamila; Kotecki, Maciej; Wojda, Alina; Szarras-Czapnik, Maria; Latos-Bielenska, Anna; Warenik-Szymankiewicz, Alina; Ruszczynska-Wolska, Anna; Jaruzelska, Jadwiga (1 Jun 1999). "Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome". Journal of Medical Genetics (بالإنجليزية). 36 (6): 452–456. DOI:10.1136/jmg.36.6.452. ISSN:0022-2593. PMC:1734388. PMID:10874632. Archived from the original on 2019-03-30.
Vetro, Annalisa; Ciccone, Roberto; Giorda, Roberto; Patricelli, Maria Grazia; Mina, Erika Della; Forlino, Antonella; Zuffardi, Orsetta (1 Jan 2011). "XX males SRY negative: a confirmed cause of infertility". Journal of Medical Genetics (بالإنجليزية). 48: jmedgenet–2011–100036. DOI:10.1136/jmedgenet-2011-100036. ISSN:0022-2593. PMC:3178810. PMID:21653197. Archived from the original on 2017-12-01.
Kurita، Masakazu؛ Aiba، Emiko؛ Matsumoto، Daisuke؛ Sato، Katsujiro؛ Nagase، Takashi؛ Yoshimura، Kotaro (مايو 2006). "Feminizing genitoplasty for treatment of XX male with masculine genitalia". Plastic and Reconstructive Surgery. ج. 117 ع. 6: 107e–111e. DOI:10.1097/01.prs.0000214653.30135.a1. ISSN:1529-4242. PMID:16651931.

ncbi.nlm.nih.gov

de la Chapelle، A (يناير 1972). "Analytic review: nature and origin of males with XX sex chromosomes". American Journal of Human Genetics. ج. 24 ع. 1: 71–105. ISSN:0002-9297. PMC:1762158. PMID:4622299.
Anık، Ahmet؛ Çatlı، Gönül؛ Abacı، Ayhan؛ Böber، Ece (2013). "46,XX Male Disorder of Sexual Development: A Case Report". Journal of Clinical Research in Pediatric Endocrinology. ج. 5 ع. 4: 258–260. DOI:10.4274/Jcrpe.1098. ISSN:1308-5727. PMC:3890225. PMID:24379036.
Lisker، R؛ Flores، F؛ Cobo، A؛ Rojas، F G (ديسمبر 1970). "A case of XX male syndrome". Journal of Medical Genetics. ج. 7 ع. 4: 394–398. DOI:10.1136/jmg.7.4.394. ISSN:0022-2593. PMC:1468937. PMID:5501706.
Kusz, Kamila; Kotecki, Maciej; Wojda, Alina; Szarras-Czapnik, Maria; Latos-Bielenska, Anna; Warenik-Szymankiewicz, Alina; Ruszczynska-Wolska, Anna; Jaruzelska, Jadwiga (1 Jun 1999). "Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome". Journal of Medical Genetics (بالإنجليزية). 36 (6): 452–456. DOI:10.1136/jmg.36.6.452. ISSN:0022-2593. PMC:1734388. PMID:10874632. Archived from the original on 2019-03-30.
Vetro, Annalisa; Ciccone, Roberto; Giorda, Roberto; Patricelli, Maria Grazia; Mina, Erika Della; Forlino, Antonella; Zuffardi, Orsetta (1 Jan 2011). "XX males SRY negative: a confirmed cause of infertility". Journal of Medical Genetics (بالإنجليزية). 48: jmedgenet–2011–100036. DOI:10.1136/jmedgenet-2011-100036. ISSN:0022-2593. PMC:3178810. PMID:21653197. Archived from the original on 2017-12-01.

omim.org (Global: 4,380^th place; Arabic: 2,257^th place)

"OMIM Entry - # 400045 - 46,XX SEX REVERSAL 1; SRXX1". www.omim.org (بالإنجليزية الأمريكية). Archived from the original on 2019-12-13. Retrieved 2017-11-07.

oup.com (Global: 485^th place; Arabic: 407^th place)

academic.oup.com

Vorona، Elena؛ Zitzmann، Michael؛ Gromoll، Jörg؛ Schüring، Andreas N.؛ Nieschlag، Eberhard (1 سبتمبر 2007). "Clinical, Endocrinological, and Epigenetic Features of the 46,XX Male Syndrome, Compared with 47,XXY Klinefelter Patients". The Journal of Clinical Endocrinology & Metabolism. ج. 92 ع. 9: 3458–3465. DOI:10.1210/jc.2007-0447. ISSN:0021-972X. مؤرشف من الأصل في 2018-07-04.
Vorona, Elena; Zitzmann, Michael; Gromoll, Jörg; Schüring, Andreas N.; Nieschlag, Eberhard (1 Sep 2007). "Clinical, Endocrinological, and Epigenetic Features of the 46,XX Male Syndrome, Compared with 47,XXY Klinefelter Patients". The Journal of Clinical Endocrinology & Metabolism (بالإنجليزية). 92 (9): 3458–3465. DOI:10.1210/jc.2007-0447. ISSN:0021-972X. Archived from the original on 2018-07-04.
Abusheikha, N.; Lass, A.; Brinsden, P. (1 Apr 2001). "XX males without SRY gene and with infertility: Case report". Human Reproduction (بالإنجليزية). 16 (4): 717–718. DOI:10.1093/humrep/16.4.717. ISSN:0268-1161. Archived from the original on 2018-07-07.
Rajender, S. (1 May 2006). "SRY-negative 46,XX male with normal genitals, complete masculinization and infertility". Molecular Human Reproduction (بالإنجليزية). 12 (5): 341–346. DOI:10.1093/molehr/gal030. ISSN:1360-9947. Archived from the original on 2019-02-24.

scielo.br (Global: 1,606^th place; Arabic: 3,279^th place)

Domenice، S.؛ Corrêa، R. V.؛ Costa، E. M. F.؛ Nishi، M. Y.؛ Vilain، E.؛ Arnhold، I. J. P.؛ Mendonca، B. B. (يناير 2004). "Mutations in the SRY, DAX1, SF1 and WNT4 genes in Brazilian sex-reversed patients". Brazilian Journal of Medical and Biological Research. ج. 37 ع. 1: 145–150. DOI:10.1590/S0100-879X2004000100020. ISSN:0100-879X. مؤرشف من الأصل في 2010-12-20.

sciencedirect.com (Global: 149^th place; Arabic: 233^rd place)

Bouayed Abdelmoula، Nouha؛ Portnoi، Marie-France؛ Keskes، Leila؛ Recan، Dominique؛ Bahloul، Ali؛ Boudawara، Tahia؛ Saad، Ali؛ Rebai، Tarek (1 يناير 2003). "Skewed X-chromosome inactivation pattern in SRY positive XX maleness: a case report and review of literature". Annales de Génétique. ج. 46 ع. 1: 11–18. DOI:10.1016/S0003-3995(03)00011-X. مؤرشف من الأصل في 2019-12-13.

web.archive.org (Global: 1^st place; Arabic: 1^st place)

Vorona، Elena؛ Zitzmann، Michael؛ Gromoll، Jörg؛ Schüring، Andreas N.؛ Nieschlag، Eberhard (1 سبتمبر 2007). "Clinical, Endocrinological, and Epigenetic Features of the 46,XX Male Syndrome, Compared with 47,XXY Klinefelter Patients". The Journal of Clinical Endocrinology & Metabolism. ج. 92 ع. 9: 3458–3465. DOI:10.1210/jc.2007-0447. ISSN:0021-972X. مؤرشف من الأصل في 2018-07-04.
Vorona, Elena; Zitzmann, Michael; Gromoll, Jörg; Schüring, Andreas N.; Nieschlag, Eberhard (1 Sep 2007). "Clinical, Endocrinological, and Epigenetic Features of the 46,XX Male Syndrome, Compared with 47,XXY Klinefelter Patients". The Journal of Clinical Endocrinology & Metabolism (بالإنجليزية). 92 (9): 3458–3465. DOI:10.1210/jc.2007-0447. ISSN:0021-972X. Archived from the original on 2018-07-04.
Abusheikha, N.; Lass, A.; Brinsden, P. (1 Apr 2001). "XX males without SRY gene and with infertility: Case report". Human Reproduction (بالإنجليزية). 16 (4): 717–718. DOI:10.1093/humrep/16.4.717. ISSN:0268-1161. Archived from the original on 2018-07-07.
Kusz, Kamila; Kotecki, Maciej; Wojda, Alina; Szarras-Czapnik, Maria; Latos-Bielenska, Anna; Warenik-Szymankiewicz, Alina; Ruszczynska-Wolska, Anna; Jaruzelska, Jadwiga (1 Jun 1999). "Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome". Journal of Medical Genetics (بالإنجليزية). 36 (6): 452–456. DOI:10.1136/jmg.36.6.452. ISSN:0022-2593. PMC:1734388. PMID:10874632. Archived from the original on 2019-03-30.
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Margarit, Ester; Coll, M. Dolors; Oliva, Rafael; Gómez, David; Soler, Anna; Ballesta, Francisca (3 Jan 2000). "SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphrodite". American Journal of Medical Genetics (بالإنجليزية). 90 (1): 25–28. DOI:10.1002/(sici)1096-8628(20000103)90:1<25::aid-ajmg5>3.0.co;2-5. ISSN:1096-8628. Archived from the original on 2023-04-19.
Aksglaede, L.; Jørgensen, N.; Skakkebæk, N. E.; Juul, A. (1 Aug 2009). "Low semen volume in 47 adolescents and adults with 47,XXY Klinefelter or 46,XX male syndrome". International Journal of Andrology (بالإنجليزية). 32 (4): 376–384. DOI:10.1111/j.1365-2605.2008.00921.x. ISSN:1365-2605. Archived from the original on 2017-12-01.

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