Mutational Analysis of the LHX1 Gene in a French National Cohort of Patients with Mayer-Rokitansky-Küster-Hauser Syndrome

D. Guerrier; N. Folléa; M. C. Voltzenlogel; L. Pasquier; K Morcel

doi:10.4172/2325-9728.1000137

Journal articles

Mutational Analysis of the LHX1 Gene in a French National Cohort of Patients with Mayer-Rokitansky-Küster-Hauser Syndrome

D. Guerrier ¹ N. Folléa M. C. Voltzenlogel L. Pasquier ^{2, 1} K Morcel ^{3, 1}

1 IGDR - Institut de Génétique et Développement de Rennes

2 Service de génétique clinique

3 Service de Gynécologie et Obstétrique [Rennes] = Gynaecology [Rennes]

Abstract : Objective: Mayer-Rokitansky-Küster-Hauser syndrome (MRKH syndrome) is characterized by congenital aplasia of the uterus and the upper part of the vagina in women showing normal secondary sexual characteristics development and a normal 46, XX ...

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Journal articles

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Life Sciences [q-bio]

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https://hal-univ-rennes1.archives-ouvertes.fr/hal-01205350
Contributor : Laurent Jonchère Connect in order to contact the contributor
Submitted on : Friday, September 25, 2015 - 1:37:10 PM
Last modification on : Friday, December 10, 2021 - 4:16:05 PM

Mutational Analysis of the LHX1 Gene in a French National Cohort of Patients with Mayer-Rokitansky-Küster-Hauser Syndrome

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Mutational Analysis of the LHX1 Gene in a French National Cohort of Patients with Mayer-Rokitansky-Küster-Hauser Syndrome

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