Edvards sindromi (Uzbek Wikipedia)

Analysis of information sources in references of the Wikipedia article "Edvards sindromi" in Uzbek language version.

refsWebsite

Global rank Uzbek rank

13nih.gov

4^th place

7^th place

12web.archive.org

1^st place

8doi.org

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3worldcat.org

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2archive.org

6^th place

8^th place

2findarticles.com

424^th place

1,945^th place

1orpha.net

3,537^th place

6,355^th place

1whonamedit.com

2,888^th place

5,667^th place

1trisomy18.org

low place

8,578^th place

1lshtm.ac.uk

low place

1emedicine.com

3,595^th place

4,001^st place

1iscn1995.org

low place

1lab-lamartine.pt

low place

1books.google.com

3^rd place

4^th place

1archive.today

14^th place

37^th place

1jamanetwork.com

2,650^th place

6,639^th place

1wrongdiagnosis.com

low place

archive.org

„Role of second trimester sonography in detecting trisomy 18: a review of 70 cases“. J Clin Ultrasound. 35-jild, № 2. 2007. 68–72-bet. doi:10.1002/jcu.20290. PMID 17206726.
Smith, David W.; Patau, Klaus; Therman, Eeva; Inhorn, Stanley L. (September 1, 1960). „A new autosomal trisomy syndrome: multiple congenital anomalies caused by an extra chromosome“. The Journal of Pediatrics. 57-jild, № 3. 338–345-bet. doi:10.1016/S0022-3476(60)80241-7. PMID 13831938.

archive.today

Zoler. „Trisomy 13 survival can exceed 1 year“. OB/GYN News (2003-yil 1-mart). 2012-yil 18-iyulda asl nusxadan arxivlangan. Qaraldi: 2008-yil 24-iyul.

books.google.com

Rodeck, Charles H.. Fetal Medicine: Basic Science and Clinical Practice. Elsevier Health Sciences, 1999. ISBN 0-443-05357-X. ^{[sayt ishlamaydi]}

doi.org

Cereda, Anna; Carey, John C (2012-10-23). „The trisomy 18 syndrome“. Orphanet Journal of Rare Diseases. 7-jild. 81-bet. doi:10.1186/1750-1172-7-81. ISSN 1750-1172. PMC 3520824. PMID 23088440.
„Role of second trimester sonography in detecting trisomy 18: a review of 70 cases“. J Clin Ultrasound. 35-jild, № 2. 2007. 68–72-bet. doi:10.1002/jcu.20290. PMID 17206726.
Imataka, George; Yamanouchi, Hideo; Arisaka, Osamu (2007). „Dandy–Walker syndrome and chromosomal abnormalities“. Congenital Anomalies (inglizcha). 47-jild, № 4. 113–118-bet. doi:10.1111/j.1741-4520.2007.00158.x. ISSN 1741-4520. PMID 17988252.
Stambolliu, Emelina; Ioakeim-Ioannidou, Myrsini; Kontokostas, Kimonas; Dakoutrou, Maria; Kousoulis, Antonis A. (2017-09-01). „The Most Common Comorbidities in Dandy-Walker Syndrome Patients: A Systematic Review of Case Reports“ (PDF). Journal of Child Neurology (inglizcha). 32-jild, № 10. 886–902-bet. doi:10.1177/0883073817712589. ISSN 0883-0738. PMID 28635420.
Nelson, Katherine E.; Rosella, Laura C.; Mahant, Sanjay; Guttmann, Astrid (2016). „Survival and Surgical Interventions for Children With Trisomy 13 and 18“. JAMA. 316-jild, № 4. 420–8-bet. doi:10.1001/jama.2016.9819. PMID 27458947. 17 November 2016da asl nusxadan arxivlandi. Qaraldi: 3 December 2016.
Edwards, J.H.; Harnden, D.G.; Cameron, A.H.; Crosse, V. Mary; Wolff, O.H. (April 9, 1960). „A new trisomic syndrome“. The Lancet. 275-jild, № 7128. 787–790-bet. doi:10.1016/S0140-6736(60)90675-9. PMID 13819419.
Smith, David W.; Patau, Klaus; Therman, Eeva; Inhorn, Stanley L. (September 1, 1960). „A new autosomal trisomy syndrome: multiple congenital anomalies caused by an extra chromosome“. The Journal of Pediatrics. 57-jild, № 3. 338–345-bet. doi:10.1016/S0022-3476(60)80241-7. PMID 13831938.
Patau, Klaus; Therman, Eeva; Smith, David W.; DeMars, Robert I. (January 19, 1961). „Trisomy for chromosome no. 18 in man“. Chromosoma. 12-jild, № 1. Berlin. 280–5-bet. doi:10.1007/BF00328924. PMID 13733243.

emedicine.com

Chen, MD. „Introduction to Trisomy 18“. EMedicine. 2008-yil 4-avgustda asl nusxadan arxivlangan. Qaraldi: 2008-yil 24-iyul.

findarticles.com

Zoler. „Trisomy 13 survival can exceed 1 year“. OB/GYN News (2003-yil 1-mart). 2012-yil 18-iyulda asl nusxadan arxivlangan. Qaraldi: 2008-yil 24-iyul.
„Trisomy 13 survival can exceed 1 year | OB/GYN News“. Find Articles (2003-yil 1-mart). 2012-yil 21-fevralda asl nusxadan arxivlangan. Qaraldi: 2012-yil 4-yanvar.

iscn1995.org

For a description of human karyotype see {{{editor}}}: „An International System for Human Cytogenetic Nomenclature“ (1995). 2006-yil 7-iyulda asl nusxadan arxivlangan. Qaraldi: 2006-yil 4-iyun.

jamanetwork.com

Nelson, Katherine E.; Rosella, Laura C.; Mahant, Sanjay; Guttmann, Astrid (2016). „Survival and Surgical Interventions for Children With Trisomy 13 and 18“. JAMA. 316-jild, № 4. 420–8-bet. doi:10.1001/jama.2016.9819. PMID 27458947. 17 November 2016da asl nusxadan arxivlandi. Qaraldi: 3 December 2016.

lab-lamartine.pt

„Prenatal Diagnose“. 2018-yil 17-avgustda asl nusxadan arxivlangan. Qaraldi: 2018-yil 17-avgust.

lshtm.ac.uk

researchonline.lshtm.ac.uk

Stambolliu, Emelina; Ioakeim-Ioannidou, Myrsini; Kontokostas, Kimonas; Dakoutrou, Maria; Kousoulis, Antonis A. (2017-09-01). „The Most Common Comorbidities in Dandy-Walker Syndrome Patients: A Systematic Review of Case Reports“ (PDF). Journal of Child Neurology (inglizcha). 32-jild, № 10. 886–902-bet. doi:10.1177/0883073817712589. ISSN 0883-0738. PMID 28635420.

nih.gov

pubmed.ncbi.nlm.nih.gov

Cereda, Anna; Carey, John C (2012-10-23). „The trisomy 18 syndrome“. Orphanet Journal of Rare Diseases. 7-jild. 81-bet. doi:10.1186/1750-1172-7-81. ISSN 1750-1172. PMC 3520824. PMID 23088440.
„[Choroid plexus cysts and risk of trisomy 18. Modifications regarding maternal age and markers]“. Ceska Gynekol (chex). 72-jild, № 1. 2007. 49–52-bet. PMID 17357350.
„Role of second trimester sonography in detecting trisomy 18: a review of 70 cases“. J Clin Ultrasound. 35-jild, № 2. 2007. 68–72-bet. doi:10.1002/jcu.20290. PMID 17206726.
Imataka, George; Yamanouchi, Hideo; Arisaka, Osamu (2007). „Dandy–Walker syndrome and chromosomal abnormalities“. Congenital Anomalies (inglizcha). 47-jild, № 4. 113–118-bet. doi:10.1111/j.1741-4520.2007.00158.x. ISSN 1741-4520. PMID 17988252.
Stambolliu, Emelina; Ioakeim-Ioannidou, Myrsini; Kontokostas, Kimonas; Dakoutrou, Maria; Kousoulis, Antonis A. (2017-09-01). „The Most Common Comorbidities in Dandy-Walker Syndrome Patients: A Systematic Review of Case Reports“ (PDF). Journal of Child Neurology (inglizcha). 32-jild, № 10. 886–902-bet. doi:10.1177/0883073817712589. ISSN 0883-0738. PMID 28635420.
Nelson, Katherine E.; Rosella, Laura C.; Mahant, Sanjay; Guttmann, Astrid (2016). „Survival and Surgical Interventions for Children With Trisomy 13 and 18“. JAMA. 316-jild, № 4. 420–8-bet. doi:10.1001/jama.2016.9819. PMID 27458947. 17 November 2016da asl nusxadan arxivlandi. Qaraldi: 3 December 2016.
Edwards, J.H.; Harnden, D.G.; Cameron, A.H.; Crosse, V. Mary; Wolff, O.H. (April 9, 1960). „A new trisomic syndrome“. The Lancet. 275-jild, № 7128. 787–790-bet. doi:10.1016/S0140-6736(60)90675-9. PMID 13819419.
Smith, David W.; Patau, Klaus; Therman, Eeva; Inhorn, Stanley L. (September 1, 1960). „A new autosomal trisomy syndrome: multiple congenital anomalies caused by an extra chromosome“. The Journal of Pediatrics. 57-jild, № 3. 338–345-bet. doi:10.1016/S0022-3476(60)80241-7. PMID 13831938.
Patau, Klaus; Therman, Eeva; Smith, David W.; DeMars, Robert I. (January 19, 1961). „Trisomy for chromosome no. 18 in man“. Chromosoma. 12-jild, № 1. Berlin. 280–5-bet. doi:10.1007/BF00328924. PMID 13733243.

nlm.nih.gov

„Trisomy 18“. Medline. 2008-yil 1-oktyabrda asl nusxadan arxivlangan. Qaraldi: 2008-yil 24-iyul.
„Trisomy 18: MedlinePlus Medical Encyclopedia“. Nlm.nih.gov (2011-yil 14-dekabr). 2012-yil 21-yanvarda asl nusxadan arxivlangan. Qaraldi: 2012-yil 4-yanvar.

ghr.nlm.nih.gov

„trisomy 18“. GHR (2012-yil mart). 2016-yil 2-oktyabrda asl nusxadan arxivlangan. Qaraldi: 2016-yil 1-oktyabr.

ncbi.nlm.nih.gov

Cereda, Anna; Carey, John C (2012-10-23). „The trisomy 18 syndrome“. Orphanet Journal of Rare Diseases. 7-jild. 81-bet. doi:10.1186/1750-1172-7-81. ISSN 1750-1172. PMC 3520824. PMID 23088440.

orpha.net

„Trisomy 18“. Orphanet (2008-yil may). 2016-yil 3-oktyabrda asl nusxadan arxivlangan. Qaraldi: 2016-yil 1-oktyabr.

trisomy18.org

„What is Trisomy 18?“. Trisomy 18 Foundation. 2009-yil 23-martda asl nusxadan arxivlangan. Qaraldi: 2008-yil 24-iyul.

web.archive.org

„trisomy 18“. GHR (2012-yil mart). 2016-yil 2-oktyabrda asl nusxadan arxivlangan. Qaraldi: 2016-yil 1-oktyabr.
„Trisomy 18“. Orphanet (2008-yil may). 2016-yil 3-oktyabrda asl nusxadan arxivlangan. Qaraldi: 2016-yil 1-oktyabr.
„Edwards syndrome (John Hilton Edwards)“. WhoNamedIt.com. 2008-yil 9-iyulda asl nusxadan arxivlangan. Qaraldi: 2008-yil 24-iyul.
„What is Trisomy 18?“. Trisomy 18 Foundation. 2009-yil 23-martda asl nusxadan arxivlangan. Qaraldi: 2008-yil 24-iyul.
„Trisomy 18“. Medline. 2008-yil 1-oktyabrda asl nusxadan arxivlangan. Qaraldi: 2008-yil 24-iyul.
Chen, MD. „Introduction to Trisomy 18“. EMedicine. 2008-yil 4-avgustda asl nusxadan arxivlangan. Qaraldi: 2008-yil 24-iyul.
For a description of human karyotype see {{{editor}}}: „An International System for Human Cytogenetic Nomenclature“ (1995). 2006-yil 7-iyulda asl nusxadan arxivlangan. Qaraldi: 2006-yil 4-iyun.
„Prenatal Diagnose“. 2018-yil 17-avgustda asl nusxadan arxivlangan. Qaraldi: 2018-yil 17-avgust.
„Trisomy 18: MedlinePlus Medical Encyclopedia“. Nlm.nih.gov (2011-yil 14-dekabr). 2012-yil 21-yanvarda asl nusxadan arxivlangan. Qaraldi: 2012-yil 4-yanvar.
„Trisomy 13 survival can exceed 1 year | OB/GYN News“. Find Articles (2003-yil 1-mart). 2012-yil 21-fevralda asl nusxadan arxivlangan. Qaraldi: 2012-yil 4-yanvar.
Nelson, Katherine E.; Rosella, Laura C.; Mahant, Sanjay; Guttmann, Astrid (2016). „Survival and Surgical Interventions for Children With Trisomy 13 and 18“. JAMA. 316-jild, № 4. 420–8-bet. doi:10.1001/jama.2016.9819. PMID 27458947. 17 November 2016da asl nusxadan arxivlandi. Qaraldi: 3 December 2016.
„Prevalence and Incidence of Edwards Syndrome“. Diseases Center-Edwards Syndrome. Adviware Pty Ltd. (2008-yil 4-fevral). — „mean maternal age for this disorder is 32½“. 2004-yil 25-iyunda asl nusxadan arxivlangan. Qaraldi: 2008-yil 17-fevral.

whonamedit.com

„Edwards syndrome (John Hilton Edwards)“. WhoNamedIt.com. 2008-yil 9-iyulda asl nusxadan arxivlangan. Qaraldi: 2008-yil 24-iyul.

worldcat.org

Cereda, Anna; Carey, John C (2012-10-23). „The trisomy 18 syndrome“. Orphanet Journal of Rare Diseases. 7-jild. 81-bet. doi:10.1186/1750-1172-7-81. ISSN 1750-1172. PMC 3520824. PMID 23088440.
Imataka, George; Yamanouchi, Hideo; Arisaka, Osamu (2007). „Dandy–Walker syndrome and chromosomal abnormalities“. Congenital Anomalies (inglizcha). 47-jild, № 4. 113–118-bet. doi:10.1111/j.1741-4520.2007.00158.x. ISSN 1741-4520. PMID 17988252.
Stambolliu, Emelina; Ioakeim-Ioannidou, Myrsini; Kontokostas, Kimonas; Dakoutrou, Maria; Kousoulis, Antonis A. (2017-09-01). „The Most Common Comorbidities in Dandy-Walker Syndrome Patients: A Systematic Review of Case Reports“ (PDF). Journal of Child Neurology (inglizcha). 32-jild, № 10. 886–902-bet. doi:10.1177/0883073817712589. ISSN 0883-0738. PMID 28635420.

wrongdiagnosis.com

„Prevalence and Incidence of Edwards Syndrome“. Diseases Center-Edwards Syndrome. Adviware Pty Ltd. (2008-yil 4-fevral). — „mean maternal age for this disorder is 32½“. 2004-yil 25-iyunda asl nusxadan arxivlangan. Qaraldi: 2008-yil 17-fevral.