J.M. Lapierre

<i>PMX2B</i>, a new candidate gene for Hirschsprung's disease

HK Benailly, J.M. Lapierre, Béatrice Laudier et al. · Clinical Genetics · 2003 · 62 citations

Chromosome 10p11.2-p12.2 duplication: Report of a patient and review of the literature

Andr� M�garban�, Philippe Gosset, Noëlle Souraty et al. · American Journal of Medical Genetics · 2001 · 50 citations

Cytogenetics, Genetics, Pathology +16

A CGH study of 27 patients with CHARGE association

Damien Sanlaville, J.M. Lapierre, Jeanne Amiel et al. · Clinical Genetics · 2002 · 34 citations

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, V Cacheux, Nathalie Collot et al. · PubMed · 1998 · 34 citations

Identification and characterization of a<i>de novo</i>partial trisomy 10p by comparative genomic hybridization (CGH)

Brigitte Benzacken, J.M. Lapierre, JP Siffroi et al. · Clinical Genetics · 1998 · 21 citations