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A novel phenotype related to partial loss of function mutations of the follicle stimulating hormone receptor.

Isabelle Beau, Philippe Touraine, G Meduri et al. · Journal of Clinical Investigation · 1998 · 274 citations · Full text

Function Mutation, Fertility, Genetics +25

New Natural Inactivating Mutations of the Follicle-Stimulating Hormone Receptor: Correlations between Receptor Function and Phenotype

Philippe Touraine, Isabelle Beau, A. Gougeon et al. · Molecular Endocrinology · 1999 · 240 citations

Genetics, Reproductive Health, Pathology +29

Fertility in Women with Nonclassical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Maud Bidet, Christine Bellanné‐Chantelot, Marie-Béatrice Galand-Portier et al. · The Journal of Clinical Endocrinology & Metabolism · 2010 · 199 citations · Full text

Delayed Puberty and Primary Amenorrhea Associated with a Novel Mutation of the Human Follicle-Stimulating Hormone Receptor: Clinical, Histological, and Molecular Studies

Geri Méduri, Philippe Touraine, Isabelle Beau et al. · The Journal of Clinical Endocrinology & Metabolism · 2003 · 184 citations · Full text

Fertility in women with late-onset adrenal hyperplasia due to 21-hydroxylase deficiency.

Steven R. Feldman, L Billaud, Jean‐Christophe Thalabard et al. · The Journal of Clinical Endocrinology & Metabolism · 1992 · 156 citations

Hormonal Contraceptive, Fertility, Reproductive Health +22