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Page 1
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: lortat jacob s. 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.
Mutation analysis of NR5A1 encoding steroidogenic factor 1 in 77 patients with 46, XY disorders of sex development (DSD) including hypospadias.
Allali S, Muller JB, Brauner R, Lourenço D, Boudjenah R, Karageorgou V, Trivin C, Lottmann H, Lortat-Jacob S, Nihoul-Fékété C, De Dreuzy O, McElreavey K, Bashamboo A. Allali S, et al. PLoS One. 2011;6(10):e24117. doi: 10.1371/journal.pone.0024117. Epub 2011 Oct 20. PLoS One. 2011. PMID: 22028768 Free PMC article.
Complete androgen insensitivity syndrome: diagnosis and management.
Cheikhelard A, Thibaud E, Morel Y, Jaubert F, Lortat-Jacob S, Polak M, Nihoul-Fekete C. Cheikhelard A, et al. Expert Rev Endocrinol Metab. 2009 Nov;4(6):565-573. doi: 10.1586/eem.09.31. Expert Rev Endocrinol Metab. 2009. PMID: 30780790
[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.
83 results