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Page 1
Anti-müllerian hormone in children with androgen insensitivity.
Rey R, Mebarki F, Forest MG, Mowszowicz I, Cate RL, Morel Y, Chaussain JL, Josso N. Rey R, et al. Among authors: chaussain jl. J Clin Endocrinol Metab. 1994 Oct;79(4):960-4. doi: 10.1210/jcem.79.4.7962305. J Clin Endocrinol Metab. 1994. PMID: 7962305
New insight into the molecular basis of 3beta-hydroxysteroid dehydrogenase deficiency: identification of eight mutations in the HSD3B2 gene eleven patients from seven new families and comparison of the functional properties of twenty-five mutant enzymes.
Moisan AM, Ricketts ML, Tardy V, Desrochers M, Mébarki F, Chaussain JL, Cabrol S, Raux-Demay MC, Forest MG, Sippell WG, Peter M, Morel Y, Simard J. Moisan AM, et al. Among authors: chaussain jl. J Clin Endocrinol Metab. 1999 Dec;84(12):4410-25. doi: 10.1210/jcem.84.12.6288. J Clin Endocrinol Metab. 1999. PMID: 10599696
Identification and characterization of the G15D mutation found in a male patient with 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) deficiency: alteration of the putative NAD-binding domain of type II 3 beta-HSD.
Rhéaume E, Sanchez R, Mébarki F, Gagnon E, Carel JC, Chaussain JL, Morel Y, Labrie F, Simard J. Rhéaume E, et al. Among authors: chaussain jl. Biochemistry. 1995 Mar 7;34(9):2893-900. doi: 10.1021/bi00009a020. Biochemistry. 1995. PMID: 7893703
Aetiological diagnosis of male sex ambiguity: a collaborative study.
Morel Y, Rey R, Teinturier C, Nicolino M, Michel-Calemard L, Mowszowicz I, Jaubert F, Fellous M, Chaussain JL, Chatelain P, David M, Nihoul-Fékété C, Forest MG, Josso N. Morel Y, et al. Among authors: chaussain jl. Eur J Pediatr. 2002 Jan;161(1):49-59. doi: 10.1007/s00431-001-0854-z. Eur J Pediatr. 2002. PMID: 11808880 Review.
287 results