Dominique Le Tessier

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

Catherine Dodé, Jacqueline Levilliers, Jean‐Michel Dupont et al. · Nature Genetics · 2003 · 830 citations

Life Sciences, Genetics, Molecular Genetics +9

Familial reciprocal translocation t(7;16) associated with maternal uniparental disomy 7 in a Silver‐Russell patient

Jean‐Michel Dupont, Laurence Cuisset, Maryse Cartigny et al. · American Journal of Medical Genetics · 2002 · 112 citations

Life Sciences, Genetics, Molecular Genetics +17

Could Digital PCR Be an Alternative as a Non-Invasive Prenatal Test for Trisomy 21: A Proof of Concept Study

Laïla El Khattabi, Christelle Rouillac-Le Sciellour, Dominique Le Tessier et al. · PLoS ONE · 2016 · 52 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Molecular cytogenetic characterization of the first reported case of inv dup del 20p compatible with a U‐type exchange model

Sandrine Leclercq, Kim Maincent, Françoise Baverel et al. · American Journal of Medical Genetics Part A · 2009 · 19 citations

Life Sciences, Genetics, Molecular Genetics +14

First reported case of intrachromosomal cryptic inv dup del Xp in a boy with developmental retardation

Céline Dupont, Aziza Lebbar, Cécile Teinturier et al. · American Journal of Medical Genetics Part A · 2007 · 14 citations

Life Sciences, Genetics, Molecular Genetics +17