Resultados de procura - J.‐C. Kaplan

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  1. 1
    Severe cystic fibrosis in a child homozygous for the G542 nonsense mutation in the CFTR gene.

    Severe cystic fibrosis in a child homozygous for the G542 nonsense mutation in the CFTR gene. por T Bienvenu, C. Beldjord, Núria Fonknechten, J.‐C. Kaplan, G. Lenoir

    Publicado 1993
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  2. 2
    Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers

    Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers por A. Haliassos, Jean‐Claude Chomel, S Grandjouan, J Kruh, J.‐C. Kaplan, Alain Kitzis

    Publicado 1989
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  3. 3
    The isolation of a human Ig Vλ gene from a recombinant library of chromosome 22 and estimation of its copy number

    The isolation of a human Ig Vλ gene from a recombinant library of chromosome 22 and estimation of its copy number por Melanie Anderson, Marie‐France Szajnert, J.‐C. Kaplan, L A McColl, Bryan D. Young

    Publicado 1984
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  4. 4
    Modification of enzymatic-ally amplified DNA for the detection of point mutations

    Modification of enzymatic-ally amplified DNA for the detection of point mutations por A. Haliassos, Jean‐Claude Chomel, Laurent Tesson, M. Baudis, J Kruh, J.‐C. Kaplan, Alain Kitzis

    Publicado 1989
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  5. 5
    Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin.

    Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin. por Kiichiro Matsumura, F.M.S. Tomé, Victor Ionâşescu, James M. Ervasti, Richard D. Anderson, Norma B. Romero, Dávid Simon, Dominique Récan, J.‐C. Kaplan, Michel Fardeau

    Publicado 1993
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  6. 6
    Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D).

    Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D). por Alain Carrié, F. Piccolo, France Leturcq, Claudia de Toma, K. Azibi, C. Beldjord, Jean‐Michel Vallat, Luciano Merlini, Thomas Voit, Caroline A. Sewry, J.A. Urtizberea, Norma B. Romero, F.M.S. Tomé, Michel Fardeau, Yoshihide Sunada, Kevin P. Campbell, J.‐C. Kaplan, Marc Jeanpierre

    Publicado 1997
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