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[Hermaphroditism pathology].
Jaubert F, Nihoul-Fékété C, Lortat-Jacob S, Josso N, Fellous M. Jaubert F, et al. Ann Pathol. 2004 Dec;24(6):499-509. doi: 10.1016/s0242-6498(04)94014-x. Ann Pathol. 2004. PMID: 15785398 Review. French.
True hermaphroditism: genetic variants and clinical management.
Hadjiathanasiou CG, Brauner R, Lortat-Jacob S, Nivot S, Jaubert F, Fellous M, Nihoul-Fékété C, Rappaport R. Hadjiathanasiou CG, et al. J Pediatr. 1994 Nov;125(5 Pt 1):738-44. doi: 10.1016/s0022-3476(94)70067-2. J Pediatr. 1994. PMID: 7965425 Clinical Trial.
Hermaphroditism pathology.
Jaubert F, Nihoul-Fékété C, Lortat-Jacob S, Josso N, Fellous M. Jaubert F, et al. Rom J Morphol Embryol. 1999-2004;45:41-51. Rom J Morphol Embryol. 1999. PMID: 15847378 Review.
Genetic mutations and somatic anomalies in association with 46,XY gonadal dysgenesis.
Bastian C, Muller JB, Lortat-Jacob S, Nihoul-Fékété C, Bignon-Topalovic J, McElreavey K, Bashamboo A, Brauner R. Bastian C, et al. Among authors: nihoul fekete c. Fertil Steril. 2015 May;103(5):1297-304. doi: 10.1016/j.fertnstert.2015.01.043. Epub 2015 Mar 23. Fertil Steril. 2015. PMID: 25813279 Free article.
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. Eur J Pediatr. 2002 Jan;161(1):49-59. doi: 10.1007/s00431-001-0854-z. Eur J Pediatr. 2002. PMID: 11808880 Review.
191 results