Genetic analyses using chromosomal microarray and exome sequencing in fetuses and women with Müllerian duct anomaliesAuriane Cospain, Sylvie Jaillard, Godeliève Morel et al.|Journal of Assisted Reproduction and Genetics|2025Cited by 2
A novel homozygous loss-of-function NOTCH3 variant in a Moroccan patient: expanding the spectrum beyond CADASILAmal Ouskri, Sylvie Jaillard, Hajar Ihlal et al.|Neurogenetics|2025Cited by 2
Role of Chromosomal Imbalances in the Pathogenesis of DSD: A Retrospective Analysis of 4657 Prenatal SamplesLaura Mary, Marc‐Antoine Belaud‐Rotureau, Mélanie Fradin et al.|SSRN Electronic Journal|2022Cited by 0