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

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 ...

Domaines: Sciences du Vivant [q-bio]

D. Guerrier, N. Folléa, M. C. Voltzenlogel, L. Pasquier, K Morcel. Mutational Analysis of the LHX1 Gene in a French National Cohort of Patients with Mayer-Rokitansky-Küster-Hauser Syndrome. Journal of Genital System & Disorders, 2015, 4 (02), pp.2. ⟨10.4172/2325-9728.1000137⟩. ⟨hal-01205350⟩