ZFHX1B mutations in patients with Mowat-Wilson syndromeFlorence Dastot‐Le Moal, Michel Goossens, Nathalie Collot et al.|Human Mutation|2007Cited by 143
Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities.J.M. Lapierre, Gérard Tachdjian, Alain Aurias et al.|PubMed|1998Cited by 34
Recurrent Intragenic Duplication within the <b><i>NR5A1</i></b> Gene and Severe Proximal HypospadiasMatthieu Peycelon, Jean‐Pierre Siffroi, Capucine Hyon et al.|Sexual Development|2017Cited by 8
Profil germinal et somatique du gène AR dans l’hypospadiasMatthieu Peycelon, Jean‐Pierre Siffroi, Florbela Frade et al.|The French Journal of Urology|2012Cited by 0