Hyon C, Chantot-Bastaraud S, Harbuz R, Bhouri R, Perrot N, Peycelon M et al. Refining the regulatory region upstream of SOX9 associated with 46,XX testicular disorders of Sex Development. DSD. Am J Med Genet A 2015; 167: 1851–1858. Article CAS Google Scholar Kim GJ, Sock E, ...
Azzi S, Salem J, Thibaud N, Chantot-Bastaraud S, Lieber E, Netchine I, et al. A prospective study validating a clinical scoring system and demonstrating phenotypical-genotypical correlations in Silver-Russell syndrome. J Med Genet. 2015;52:446–53. Article CAS PubMed PubMed Central Google...
Chantot-Bastaraud, A. Faudet, et al. 2014. Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders. Eur. J. Hum. Genet. 22:71-78.Nava C, Keren B, Mignot C, Rastetter A, Chantot-Bastaraud S, Faudet A, Fonteneau E, ...
copy_m4_m4(pchanto->chan_mat, pchanfrom->chan_mat);/* used for local constraints */copy_v3_v3(pchanto->loc, pchanfrom->loc);copy_qt_qt(pchanto->quat, pchanfrom->quat); copy_v3_v3(pchanto->eul, pchanfrom->eul); copy_v3_v3(pchanto->size, pchanfrom->size); copy_v3_v3(...
Reading and language skills have overlapping genetic bases, most of which are still unknown. Part of the missing heritability may be caused by copy number variants (CNVs). In a dataset of children recruited for a history of reading disability (RD, also k
Nava C, Keren B, Mignot C, Rastetter A, Chantot-Bastaraud S, Faudet A, Fonteneau E, Amiet C, Laurent C, Jacquette A, et al. (2013). Prospec- tive diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders. Eur J Hum Genet 22, ...