Torthaí cuardaigh - 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. de réir T Bienvenu, C. Beldjord, Núria Fonknechten, J.‐C. Kaplan, G. Lenoir

    Foilsithe / Cruthaithe 1993
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    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 de réir A. Haliassos, Jean‐Claude Chomel, S Grandjouan, J Kruh, J.‐C. Kaplan, Alain Kitzis

    Foilsithe / Cruthaithe 1989
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    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 de réir Melanie Anderson, Marie‐France Szajnert, J.‐C. Kaplan, L A McColl, Bryan D. Young

    Foilsithe / Cruthaithe 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 de réir A. Haliassos, Jean‐Claude Chomel, Laurent Tesson, M. Baudis, J Kruh, J.‐C. Kaplan, Alain Kitzis

    Foilsithe / Cruthaithe 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. de réir 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

    Foilsithe / Cruthaithe 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). de réir 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

    Foilsithe / Cruthaithe 1997
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