Works matching IS 09646906 AND DT 2012 AND VI 21 AND IP 7


Results: 24
    1

    Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 7, p. 1513, doi. 10.1093/hmg/ddr589
    By:
    • Soemedi, Rachel;
    • Topf, Ana;
    • Wilson, Ian J.;
    • Darlay, Rebecca;
    • Rahman, Thahira;
    • Glen, Elise;
    • Hall, Darroch;
    • Huang, Ni;
    • Bentham, Jamie;
    • Bhattacharya, Shoumo;
    • Cosgrove, Catherine;
    • Brook, J. David;
    • Granados-Riveron, Javier;
    • Setchfield, Kerry;
    • Bu'Lock, Frances;
    • Thornborough, Chris;
    • Devriendt, Koenraad;
    • Breckpot, Jeroen;
    • Hofbeck, Michael;
    • Lathrop, Mark
    Publication type:
    Article
    2

    A genome-wide association study identifies locus at 10q22 associated with clinical outcomes of adjuvant tamoxifen therapy for breast cancer patients in Japanese.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 7, p. 1665, doi. 10.1093/hmg/ddr597
    By:
    • Kiyotani, Kazuma;
    • Mushiroda, Taisei;
    • Tsunoda, Tatsuhiko;
    • Morizono, Takashi;
    • Hosono, Naoya;
    • Kubo, Michiaki;
    • Tanigawara, Yusuke;
    • Imamura, Chiyo K.;
    • Flockhart, David A.;
    • Aki, Fuminori;
    • Hirata, Koichi;
    • Takatsuka, Yuichi;
    • Okazaki, Minoru;
    • Ohsumi, Shozo;
    • Yamakawa, Takashi;
    • Sasa, Mitsunori;
    • Nakamura, Yusuke;
    • Zembutsu, Hitoshi
    Publication type:
    Article
    3
    4

    Lafora bodies and neurological defects in malin-deficient mice correlate with impaired autophagy.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 7, p. 1521, doi. 10.1093/hmg/ddr590
    By:
    • Criado, Olga;
    • Aguado, Carmen;
    • Gayarre, Javier;
    • Duran-Trio, Lara;
    • Garcia-Cabrero, Ana M.;
    • Vernia, Santiago;
    • San Millán, Beatriz;
    • Heredia, Miguel;
    • Romá-Mateo, Carlos;
    • Mouron, Silvana;
    • Juana-López, Lucía;
    • Domínguez, Mercedes;
    • Navarro, Carmen;
    • Serratosa, Jose M.;
    • Sanchez, Marina;
    • Sanz, Pascual;
    • Bovolenta, Paola;
    • Knecht, Erwin;
    • Rodriguez de Cordoba, Santiago
    Publication type:
    Article
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    Subscription Page.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 7, p. NP, doi. 10.1093/hmg/dds077
    Publication type:
    Article
    9

    Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 7, p. 1496, doi. 10.1093/hmg/ddr585
    By:
    • Narisawa, Ayumi;
    • Komatsuzaki, Shoko;
    • Kikuchi, Atsuo;
    • Niihori, Tetsuya;
    • Aoki, Yoko;
    • Fujiwara, Kazuko;
    • Tanemura, Mitsuyo;
    • Hata, Akira;
    • Suzuki, Yoichi;
    • Relton, Caroline L.;
    • Grinham, James;
    • Leung, Kit-Yi;
    • Partridge, Darren;
    • Robinson, Alexis;
    • Stone, Victoria;
    • Gustavsson, Peter;
    • Stanier, Philip;
    • Copp, Andrew J.;
    • Greene, Nicholas D.E.;
    • Tominaga, Teiji
    Publication type:
    Article
    10
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    Contents Page.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 7, p. NP, doi. 10.1093/hmg/dds074
    Publication type:
    Article
    13

    Post-genome wide association studies and functional analyses identify association of MPP7 gene variants with site-specific bone mineral density.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 7, p. 1648, doi. 10.1093/hmg/ddr586
    By:
    • Xiao, Su-Mei;
    • Kung, Annie Wai Chee;
    • Gao, Yi;
    • Lau, Kam-Shing;
    • Ma, Alvin;
    • Zhang, Zhen-Lin;
    • Liu, Jian-Min;
    • Xia, Wiebo;
    • He, Jin-Wei;
    • Zhao, Lin;
    • Nie, Min;
    • Fu, Wei-Zhen;
    • Zhang, Min-Jia;
    • Sun, Jing;
    • Kwan, Johnny S.H.;
    • Tso, Gloria Hoi Wan;
    • Dai, Zhi-Jie;
    • Cheung, Ching-Lung;
    • Bow, Cora H.;
    • Leung, Anskar Yu Hung
    Publication type:
    Article
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    Editorial Board.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 7, p. NP, doi. 10.1093/hmg/dds076
    Publication type:
    Article
    23
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    Cover Page.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 7, p. NP, doi. 10.1093/hmg/dds075
    Publication type:
    Article