J. Lespinasse

Non-disjunction of chromosome 13

Merete Bugge, Andrew Collins, Jens Michael Hertz et al. · Human Molecular Genetics · 2007 · 118 citations · Full text

Cytogenetics, Genetics, Molecular Genetics +18

Phenotypic and genotypic variability in monozygotic triplets with Turner syndrome

J. Lespinasse, Christine Gicquel, M Robert et al. · Clinical Genetics · 1998 · 96 citations

Karyotype Imaging, Developmental Biology, Mendelian Disorder +15

Chromosomal instability in two siblings with gonad deficiency: Case report

J. Lespinasse, P. Hoffmann, Anthony Laugé et al. · Human Reproduction · 2004 · 74 citations · Full text

Rare Robertsonian translocations and meiotic behaviour: sperm FISH analysis of t(13;15) and t(14;15) translocations: A Case Report

Kamran Moradkhani, Jacques Puechberty, Samarth Bhatt et al. · Human Reproduction · 2006 · 67 citations · Full text

Fertility, Cytogenetics, Genetics +17

A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes

Justine Besseau-Ayasse, C. Violle-Poirsier, Anne Bazin et al. · Prenatal Diagnosis · 2014 · 59 citations