Ngā hua rapu - 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. mā T Bienvenu, C. Beldjord, Núria Fonknechten, J.‐C. Kaplan, G. Lenoir

    I whakaputaina 1993
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Carta
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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 mā A. Haliassos, Jean‐Claude Chomel, S Grandjouan, J Kruh, J.‐C. Kaplan, Alain Kitzis

    I whakaputaina 1989
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Melanie Anderson, Marie‐France Szajnert, J.‐C. Kaplan, L A McColl, Bryan D. Young

    I whakaputaina 1984
    Whiwhi kuputuhi katoa
    Artigo
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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 mā A. Haliassos, Jean‐Claude Chomel, Laurent Tesson, M. Baudis, J Kruh, J.‐C. Kaplan, Alain Kitzis

    I whakaputaina 1989
    Whiwhi kuputuhi katoa
    Artigo
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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. mā 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

    I whakaputaina 1993
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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). mā 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

    I whakaputaina 1997
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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