C. Mignon

The human EZH2 gene: genomic organisation and revised mapping in 7q35 within the critical region for malignant myeloid disorders

Carlos Cardoso, C. Mignon, Gilles Hetet et al. · European Journal of Human Genetics · 2000 · 111 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Cloning, Chromosomal Localization, and Physical Linkage of the β and γ Subunits (SCNN1B and SCNN1G) of the Human Epithelial Amiloride-Sensitive Sodium Channel

Nicolas Voilley, Frédéric Bassilana, C. Mignon et al. · Genomics · 1995 · 78 citations

Natural Sciences, Genetics, Molecular Biology +17

Clinical Heterogeneity in 16 Patientswith inv dup 15 Chromosome:Cytogenetic and Molecular Studies,Search for an Imprinting Effect

C. Mignon, Perrine Malzac, A. Moncla et al. · European Journal of Human Genetics · 1996 · 69 citations

Life Sciences, Genetics, Molecular Genetics +13

Mapping of the galectin-3 gene (LGALS3) to human Chromosome 14 at region 14q21-22

Jacques Raimond, Drazen B. Zimonjic, C. Mignon et al. · Mammalian Genome · 1997 · 66 citations

Life Sciences, Genetics, Molecular Genetics +6

The mouse Necdin gene is expressed from the paternal allele only and lies in the 7C region of the mouse chromosome 7, a region of conserved synteny to the human Prader-Willi syndrome region.

Françoise Watrin, Nathalie Roëckel, Laurence Lacroix et al. · PubMed · 1998 · 38 citations

Life Sciences, Genetics, Molecular Genetics +8