Works matching IS 09646906 AND DT 2012 AND VI 21 AND IP 5


Results: 25
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    Cover Page.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 5, p. NP, doi. 10.1093/hmg/dds042
    Publication type:
    Article
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    A glial origin for periventricular nodular heterotopia caused by impaired expression of Filamin-A.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 5, p. 1004, doi. 10.1093/hmg/ddr531
    By:
    • Carabalona, Aurelie;
    • Beguin, Shirley;
    • Pallesi-Pocachard, Emilie;
    • Buhler, Emmanuelle;
    • Pellegrino, Christophe;
    • Arnaud, Karen;
    • Hubert, Philippe;
    • Oualha, Mehdi;
    • Siffroi, Jean Pierre;
    • Khantane, Sabrina;
    • Coupry, Isabelle;
    • Goizet, Cyril;
    • Gelot, Antoinette Bernabe;
    • Represa, Alfonso;
    • Cardoso, Carlos
    Publication type:
    Article
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    The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 5, p. 1190, doi. 10.1093/hmg/ddr551
    By:
    • Han, Summer S.;
    • Yeager, Meredith;
    • Moore, Lee E.;
    • Wei, Ming-Hui;
    • Pfeiffer, Ruth;
    • Toure, Ousmane;
    • Purdue, Mark P.;
    • Johansson, Mattias;
    • Scelo, Ghislaine;
    • Chung, Charles C.;
    • Gaborieau, Valerie;
    • Zaridze, David;
    • Schwartz, Kendra;
    • Szeszenia-Dabrowska, Neonilia;
    • Davis, Faith;
    • Bencko, Vladimir;
    • Colt, Joanne S.;
    • Janout, Vladimir;
    • Matveev, Vsevolod;
    • Foretova, Lenka
    Publication type:
    Article
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    Contents Page.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 5, p. NP, doi. 10.1093/hmg/dds041
    Publication type:
    Article
    16

    Subscription Page.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 5, p. NP, doi. 10.1093/hmg/dds044
    Publication type:
    Article
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    Editorial Board.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 5, p. NP, doi. 10.1093/hmg/dds043
    Publication type:
    Article
    20

    Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 5, p. 1184, doi. 10.1093/hmg/ddr550
    By:
    • Guo, Youling;
    • Baum, Larry W.;
    • Sham, Pak Chung;
    • Wong, Virginia;
    • Ng, Ping Wing;
    • Lui, Colin Hiu Tung;
    • Sin, Ngai Chuen;
    • Tsoi, Tak Hong;
    • Tang, Clara S.M.;
    • Kwan, Johnny S.H.;
    • Yip, Benjamin H.K.;
    • Xiao, Su-Mei;
    • Thomas, G. Neil;
    • Lau, Yu Lung;
    • Yang, Wanling;
    • Cherny, Stacey S.;
    • Kwan, Patrick
    Publication type:
    Article
    21

    DelK32-lamin A/C has abnormal location and induces incomplete tissue maturation and severe metabolic defects leading to premature death.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 5, p. 1037, doi. 10.1093/hmg/ddr534
    By:
    • Bertrand, Anne T.;
    • Renou, Laure;
    • Papadopoulos, Aurélie;
    • Beuvin, Maud;
    • Lacène, Emmanuelle;
    • Massart, Catherine;
    • Ottolenghi, Chris;
    • Decostre, Valérie;
    • Maron, Sophia;
    • Schlossarek, Saskia;
    • Cattin, Marie-Elodie;
    • Carrier, Lucie;
    • Malissen, Marie;
    • Arimura, Takuro;
    • Bonne, Gisèle
    Publication type:
    Article
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