Françoise Baverel

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

Catherine Dodé, Jacqueline Levilliers, Jean‐Michel Dupont et al. · Nature Genetics · 2003 · 825 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +3

Pure familial 6q21q22.1 duplication in two generations

Mohammad Pazooki, Aziza Lebbar, Anne Roubergues et al. · European Journal of Medical Genetics · 2006 · 85 citations

Pure Familial 6Q21q22.1, Genetic Disorder, Genetics +4

First cryptic balanced reciprocal translocation mosaicism and familial transmission

Céline Dupont, Andrée Delahaye‐Duriez, Lydie Bürglen et al. · American Journal of Medical Genetics Part A · 2008 · 72 citations

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

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