Mutational analysis of the WNT gene family in women with Mayer-Rokitansky-Kuster-Hauser syndrome

Author:

Ravel Celia,Lorenço Diana,Dessolle Lionel,Mandelbaum Jacqueline,McElreavey Ken,Darai Emile,Siffroi Jean Pierre

Funder

Association pour la Recherche sur le Cancer

GIS-Institut des Maladies Rares

March of Dimes Foundation

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology,Reproductive Medicine

Reference17 articles.

1. Programme de Recherches sur les Aplasies Müllériennes. Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome;Morcel;Orphanet J Rare Dis,2007

2. WNT4 deficiency—a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case report;Biason-Lauber;Hum Reprod,2007

3. Multiplicity of the interactions of Wnt proteins and their receptors;Kikuchi;Cell Signal,2007

4. Female development in mammals is regulated by Wnt-4 signaling;Vainio;Nature,1999

5. A WNT4 mutation associated with müllerian-duct regression and virilization in a 46,XX woman;Biason-Lauber;N Engl J Med,2004

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