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228 results

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Page 1
Persistence of Müllerian remnants in complete androgen insensitivity syndrome.
Damiani D, Mascolli MA, Almeida MJ, Jaubert F, Fellous M, Dichtchekenian V, Tobo PR, Moreira-Filho CA, Setian N. Damiani D, et al. Among authors: jaubert f. J Pediatr Endocrinol Metab. 2002 Nov-Dec;15(9):1553-6. doi: 10.1515/jpem.2002.15.9.1553. J Pediatr Endocrinol Metab. 2002. PMID: 12503865
The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumor.
Barbosa AS, Hadjiathanasiou CG, Theodoridis C, Papathanasiou A, Tar A, Merksz M, Györvári B, Sultan C, Dumas R, Jaubert F, Niaudet P, Moreira-Filho CA, Cotinot C, Fellous M. Barbosa AS, et al. Among authors: jaubert f. Hum Mutat. 1999;13(2):146-53. doi: 10.1002/(SICI)1098-1004(1999)13:2<146::AID-HUMU7>3.0.CO;2-I. Hum Mutat. 1999. PMID: 10094551
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.
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: jaubert f. Eur J Pediatr. 2002 Jan;161(1):49-59. doi: 10.1007/s00431-001-0854-z. Eur J Pediatr. 2002. PMID: 11808880 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: jaubert f. 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.
Evaluation of gonadal function in 107 intersex patients by means of serum antimüllerian hormone measurement.
Rey RA, Belville C, Nihoul-Fékété C, Michel-Calemard L, Forest MG, Lahlou N, Jaubert F, Mowszowicz I, David M, Saka N, Bouvattier C, Bertrand AM, Lecointre C, Soskin S, Cabrol S, Crosnier H, Léger J, Lortat-Jacob S, Nicolino M, Rabl W, Toledo SP, Baş F, Gompel A, Czernichow P, Josso N, et al. Rey RA, et al. Among authors: jaubert f. J Clin Endocrinol Metab. 1999 Feb;84(2):627-31. doi: 10.1210/jcem.84.2.5507. J Clin Endocrinol Metab. 1999. PMID: 10022428
Molecular genetics of sex determination.
Cotinot C, Pailhoux E, Jaubert F, Fellous M. Cotinot C, et al. Among authors: jaubert f. Semin Reprod Med. 2002 Aug;20(3):157-68. doi: 10.1055/s-2002-35380. Semin Reprod Med. 2002. PMID: 12428196 Review.
[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.
228 results