Works matching IS 10184813 AND DT 2013 AND VI 21 AND IP 9

Results: 27
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    Genes identified in Asian SLE GWASs are also associated with SLE in Caucasian populations.

    Published in:
    European Journal of Human Genetics, 2013, v. 21, n. 9, p. 994, doi. 10.1038/ejhg.2012.277
    By:
    • Wang, Chuan;
    • Ahlford, Annika;
    • Järvinen, Tiina M;
    • Nordmark, Gunnel;
    • Eloranta, Maija-Leena;
    • Gunnarsson, Iva;
    • Svenungsson, Elisabet;
    • Padyukov, Leonid;
    • Sturfelt, Gunnar;
    • Jönsen, Andreas;
    • Bengtsson, Anders A;
    • Truedsson, Lennart;
    • Eriksson, Catharina;
    • Rantapää-Dahlqvist, Solbritt;
    • Sjöwall, Christopher;
    • Julkunen, Heikki;
    • Criswell, Lindsey A;
    • Graham, Robert R;
    • Behrens, Timothy W;
    • Kere, Juha
    Publication type:
    Article
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    Mosaic copy number variation in schizophrenia.

    Published in:
    European Journal of Human Genetics, 2013, v. 21, n. 9, p. 1007, doi. 10.1038/ejhg.2012.287
    By:
    • Ruderfer, Douglas M;
    • Chambert, Kim;
    • Moran, Jennifer;
    • Talkowski, Michael;
    • Chen, Elizabeth S;
    • Gigek, Carolina;
    • Gusella, James F;
    • Blackwood, Douglas H;
    • Corvin, Aiden;
    • Gurling, Hugh M;
    • Hultman, Christina M;
    • Kirov, George;
    • Magnusson, Patrick;
    • O'Donovan, Michael C;
    • Owen, Michael J;
    • Pato, Carlos;
    • St Clair, David;
    • Sullivan, Patrick F;
    • Purcell, Shaun M;
    • Sklar, Pamela
    Publication type:
    Article
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    André Boué (1925-2012).

    Published in:
    European Journal of Human Genetics, 2013, v. 21, n. 9, p. 893, doi. 10.1038/ejhg.2013.127
    By:
    • Gilgenkrantz, Simone;
    • Junien, Claudine
    Publication type:
    Article
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    Custom oligonucleotide array-based CGH: a reliable diagnostic tool for detection of exonic copy-number changes in multiple targeted genes.

    Published in:
    European Journal of Human Genetics, 2013, v. 21, n. 9, p. 977, doi. 10.1038/ejhg.2012.279
    By:
    • Vasson, Aurélie;
    • Leroux, Céline;
    • Orhant, Lucie;
    • Boimard, Mathieu;
    • Toussaint, Aurélie;
    • Leroy, Chrystel;
    • Commere, Virginie;
    • Ghiotti, Tiffany;
    • Deburgrave, Nathalie;
    • Saillour, Yoann;
    • Atlan, Isabelle;
    • Fouveaut, Corinne;
    • Beldjord, Cherif;
    • Valleix, Sophie;
    • Leturcq, France;
    • Dodé, Catherine;
    • Bienvenu, Thierry;
    • Chelly, Jamel;
    • Cossée, Mireille
    Publication type:
    Article
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    Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease.

    Published in:
    European Journal of Human Genetics, 2013, v. 21, n. 9, p. 1031, doi. 10.1038/ejhg.2013.91
    By:
    • Shanks, Morag E;
    • Downes, Susan M;
    • Copley, Richard R;
    • Lise, Stefano;
    • Broxholme, John;
    • Hudspith, Karl A Z;
    • Kwasniewska, Alexandra;
    • Davies, Wayne I L;
    • Hankins, Mark W;
    • Packham, Emily R;
    • Clouston, Penny;
    • Seller, Anneke;
    • Wilkie, Andrew O M;
    • Taylor, Jenny C;
    • Ragoussis, Jiannis;
    • Németh, Andrea H
    Publication type:
    Article
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    Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings.

    Published in:
    European Journal of Human Genetics, 2013, v. 21, n. 9, p. 936, doi. 10.1038/ejhg.2012.285
    By:
    • Croonen, Ellen A;
    • Nillesen, Willy M;
    • Stuurman, Kyra E;
    • Oudesluijs, Gretel;
    • van de Laar, Ingrid M B M;
    • Martens, Liesbeth;
    • Ockeloen, Charlotte;
    • Mathijssen, Inge B;
    • Schepens, Marga;
    • Ruiterkamp-Versteeg, Martina;
    • Scheffer, Hans;
    • Faas, Brigitte H W;
    • van der Burgt, Ineke;
    • Yntema, Helger G
    Publication type:
    Article
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