Identification of Candidate Genes for Mayer-Rokitansky-Küster-Hauser Syndrome Using Genomic Approaches-Reference-Cited by-同舟云学术

Identification of Candidate Genes for Mayer-Rokitansky-Küster-Hauser Syndrome Using Genomic Approaches

Published:2018-12-01 Issue:1 Volume:13 Page:26-34
ISSN:1661-5425
Container-title:Sexual Development
language:en
Short-container-title:Sex Dev

Author:

Backhouse Brendan,Hanna Chloe,Robevska Gorjana,van den Bergen Jocelyn,Pelosi Emanuele,Simons Cas,Koopman Peter,Juniarto A. Zulfa,Grover Sonia,Faradz Sultana,Sinclair Andrew,Ayers Katie,Tan Tiong Y.

Publisher

S. Karger AG

Subject

Developmental Biology,Embryology,Endocrinology, Diabetes and Metabolism

Reference34 articles.

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2. Biason-Lauber A, Konrad D, Navratil F, Schoenle EJ: A WNT4 mutation associated with Müllerian-duct regression and virilization in a 46,XX woman. N Engl J Med 351:792-798 (2004).

3. Bingham C, Ellard S, Cole TRP, Jones KE, Allen LIS, et al: Solitary functioning kidney and diverse genital tract malformations associated with hepatocyte nuclear factor-1beta mutations. Kidney Int 61:1243-1251 (2002).

4. Bombard DS, Mousa SA: Mayer-Rokitansky-Kuster-Hauser syndrome: complications, diagnosis and possible treatment options: a review. Gynecol Endocrinol 30:618-623 (2014).

5. Brucker SY, Frank L, Eisenbeis S, Henes M, Wallwiener D, et al: Sequence variants in ESR1 and OXTR are associated with Mayer-Rokitansky-Küster-Hauser syndrome. Acta Obstet Gynecol Scand 96:1338-1346 (2017).

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