A. Moncla

Mutation Analysis of UBE3A in Angelman Syndrome Patients

Perrine Malzac, Hayley Webber, A. Moncla et al. · The American Journal of Human Genetics · 1998 · 218 citations · Full text

Mendelian Disorder, Genetic Disorder, Medicine +6

DNMT3B mutations and DNA methylation defect define two types of ICF syndrome

Yanyan Jiang, Muriel Rigolet, Déborah Bourc’his et al. · Human Mutation · 2004 · 132 citations

Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletion

Carlos Cardoso, Amber Boys, Elena Parrini et al. · Neurology · 2008 · 129 citations

PML nuclear bodies are highly organised DNA-protein structures with a function in heterochromatin remodelling at the G2 phase

Judith Luciani, D. Depétris, Yves Usson et al. · Journal of Cell Science · 2006 · 125 citations

Dna, Nuclear Structure, Satellite Dna +20

Triplet repeat expansion at the FRAXE locus and X-linked mild mental handicap.

Samantha J.L. Knight, Marie‐Antoinette Voelckel, Mark C. Hirst et al. · PubMed · 1994 · 119 citations