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[Hermaphroditism pathology].
Jaubert F, Nihoul-Fékété C, Lortat-Jacob S, Josso N, Fellous M. Jaubert F, et al. Among authors: fellous m. Ann Pathol. 2004 Dec;24(6):499-509. doi: 10.1016/s0242-6498(04)94014-x. Ann Pathol. 2004. PMID: 15785398 Review. French.
Hermaphroditism pathology.
Jaubert F, Nihoul-Fékété C, Lortat-Jacob S, Josso N, Fellous M. Jaubert F, et al. Among authors: fellous m. Rom J Morphol Embryol. 1999-2004;45:41-51. Rom J Morphol Embryol. 1999. PMID: 15847378 Review.
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. Among authors: fellous m. 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.
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: fellous m. Eur J Pediatr. 2002 Jan;161(1):49-59. doi: 10.1007/s00431-001-0854-z. Eur J Pediatr. 2002. PMID: 11808880 Review.
Donor splice-site mutations in WT1 are responsible for Frasier syndrome.
Barbaux S, Niaudet P, Gubler MC, Grünfeld JP, Jaubert F, Kuttenn F, Fékété CN, Souleyreau-Therville N, Thibaud E, Fellous M, McElreavey K. Barbaux S, et al. Among authors: fellous m. Nat Genet. 1997 Dec;17(4):467-70. doi: 10.1038/ng1297-467. Nat Genet. 1997. PMID: 9398852
Foxl-2 in gonad development and pathology.
Jaubert F, Galmiche L, Lortat-Jacob S, Fournet JC, Fellous M. Jaubert F, et al. Among authors: fellous m. Arkh Patol. 2011 Jul-Aug;73(4):10-3. Arkh Patol. 2011. PMID: 22164424 Review.
304 results