J.‐C. Kaplan

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.

Alan H. Beggs, Mary B. Moyer, S. Scherpf et al. · PubMed · 1989 · 961 citations

Modification of enzymatic-ally amplified DNA for the detection of point mutations

A. Haliassos, Jean‐Claude Chomel, Laurent Tesson et al. · Nucleic Acids Research · 1989 · 322 citations

Engineering, Genetics, Dna Analysis +17

Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers

A. Haliassos, Jean‐Claude Chomel, S Grandjouan et al. · Nucleic Acids Research · 1989 · 178 citations · Full text

Genetics, Dna Analysis, Pathology +24

Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D).

Alain Carrié, Fédérica Piccolo, France Leturcq et al. · Journal of Medical Genetics · 1997 · 115 citations · Full text

Rare Diseases, Mendelian Disorder, Genetic Disorder +13

The isolation of a human Ig Vλ gene from a recombinant library of chromosome 22 and estimation of its copy number

Melanie Anderson, Marie‐France Szajnert, J.‐C. Kaplan et al. · Nucleic Acids Research · 1984 · 93 citations · Full text