Farida Mébarki

Congenital adrenal hyperplasia due to point mutations in the type II 3β–hydroxysteroid dehydrogenase gene

Éric Rhéaume, Jacques Simard, Yves Morel et al. · Nature Genetics · 1992 · 235 citations

Adrenal Gland, Developmental Biology, Type Ii 3β–Hydroxysteroid +9

Anti-müllerian hormone in children with androgen insensitivity.

Rodolfo A. Rey, Farida Mébarki, Maguelone G. Forest et al. · The Journal of Clinical Endocrinology & Metabolism · 1994 · 113 citations

Serum Amh Concentration, Fertility, Reproductive Health +17

New Insight into the Molecular Basis of 3β-Hydroxysteroid Dehydrogenase Deficiency: Identification of Eight Mutations in the HSD3B2 Gene in Eleven Patients from Seven New Families and Comparison of the Functional Properties of Twenty-Five Mutant Enzymes1

Anne Marie Moisan, Marie‐Louise Ricketts, Véronique Tardy et al. · The Journal of Clinical Endocrinology & Metabolism · 1999 · 105 citations · Full text

Different phenotypes in a family with androgen insensitivity caused by the same M780I point mutation in the androgen receptor gene.

Patrice Rodien, Farida Mébarki, I Mowszowicz et al. · The Journal of Clinical Endocrinology & Metabolism · 1996 · 78 citations · Full text

Androgen Receptor, Genetics, Human Polymorphism +22

Molecular biology and genetics of the 3 beta-hydroxysteroid dehydrogenase/delta5-delta4 isomerase gene family.

Jacques Simard, Francine Durocher, Farida Mébarki et al. · PubMed · 1996 · 72 citations

Natural Sciences, Genetics, Gene Structure +7