Journal of Genital System & DisordersISSN: 2325-9728

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Foll�a N Author

daniel.guerrier@univrennes1.fr

Subjects of specialization
 LHX1 Gene; Mayer-Rokitansky-Küster-Hauser syndrome; Müllerian aplasia; Genetic disease; Congenital malformation; Mutational analysis

Affiliation
CNRS UMR 6290

Biography

Follï N is working in a CNRS UMR 6290 – Institute for Genetics and Development of Rennes (IGDR), F-35043 Rennes, France. He has published more number of articles and he has the good knowledge in Mayer-Rokitansky-Küster-Hauser syndrome; Müllerian aplasia; Genetic disease; Congenital malformation; Mutational analysis, Cesarean scar pregnancy; Ectopic pregnancy; Treatment.

Publications

Research Article Subscription

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

Author(s):

Guerrier D, Foll�a N, Voltzenlogel M-C, Pasquier L and Morcel K

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

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 karyotype. MRKH syndrome is a cause of primary amenorrhea with an incidence of appro... view more»

DOI: 10.4172/2325-9728.1000137

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