Identification and Characterization of Novel <scp>FSHR</scp> Copy Number Variations Causing Premature Ovarian Insufficiency
Anna Lokchine(Inserm), Sylvie Jaillard(Inserm), Mathilde Domin‐Bernhard(Centre Hospitalier Universitaire de Rennes), Linda Akloul(Centre Hospitalier Universitaire de Rennes), Marc‐Antoine Belaud‐Rotureau(Inserm), Erika Launay(Université Sorbonne Paris Nord), Anne Bergougnoux(Centre National de la Recherche Scientifique), Laura Mary(Inserm), Elena J. Tucker(The University of Melbourne), Solène Duros(Centre Hospitalier Universitaire de Rennes), Françoise Paris(Université de Montpellier), Sylvie Odent(Centre National de la Recherche Scientifique), Mathieu Philippe(Centre Hospitalier Universitaire de Rennes), Nadège Servant(Université de Montpellier), Laurence Cluzeau(Centre Hospitalier Universitaire de Rennes)
Cited by 1
Related Papers
Phenotypical, Biological, and Molecular Heterogeneity of 5α-Reductase Deficiency: An Extensive International Experience of 55 Patients
|The Journal of Clinical Endocrinology & Metabolism|2010|213
Activating Mutations of the Stimulatory G Protein in Juvenile Ovarian Granulosa Cell Tumors: A New Prognostic Factor?
|The Journal of Clinical Endocrinology & Metabolism|2006|109
GJB2 and GJB6 Mutations
|Archives of Otolaryngology - Head and Neck Surgery|2005|104
Molecular Diagnosis of 5α-Reductase Deficiency in 4 Elite Young Female Athletes Through Hormonal Screening for Hyperandrogenism
|The Journal of Clinical Endocrinology & Metabolism|2013|71