Výsledky vyhledávání - Martin J. Somerville

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  1. 1
    GDF6, a Novel Locus for a Spectrum of Ocular Developmental Anomalies

    GDF6, a Novel Locus for a Spectrum of Ocular Developmental Anomalies Autor Mika Asai-Coakwell, Curtis R. French, K. Berry, Ming Ye, Ron Koss, Martin J. Somerville, Rosemary Mueller, Veronica van Heyningen, Andrew J. Waskiewicz, Ordan J. Lehmann

    Vydáno 2007
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  2. 2
    Chromosome 1q21.1 Contiguous Gene Deletion Is Associated With Congenital Heart Disease

    Chromosome 1q21.1 Contiguous Gene Deletion Is Associated With Congenital Heart Disease Autor Jesse Christiansen, John D. Dyck, Basil G. Elyas, Margaret Lilley, J. Bamforth, Mark Hicks, Kathleen A. Sprysak, Robert Tomaszewski, Shelagh Haase, Leanne M. Vicen-Wyhony, Martin J. Somerville

    Vydáno 2004
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  3. 3
    Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss

    Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss Autor Evica Rajcan‐Separovic, Dan Diego‐Álvarez, Wendy P. Robinson, Christine Tyson, Ying Qiao, Chansonette Harvard, Chris Fawcett, Dagmar K. Kalousek, Tom Philipp, Martin J. Somerville, Mary D. Stephenson

    Vydáno 2010
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  4. 4
    Severe Expressive-Language Delay Related to Duplication of the Williams–Beuren Locus

    Severe Expressive-Language Delay Related to Duplication of the Williams–Beuren Locus Autor Martin J. Somerville, Carolyn Β. Mervis, Edwin J. Young, Eul‐Ju Seo, Miguel Del Campo, Stephen Bamforth, Ella Peregrine, Wayne Loo, Margaret Lilley, Luis A. Pérez‐Jurado, Colleen A. Morris, Stephen W. Scherer, Lucy R. Osborne

    Vydáno 2005
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  5. 5
    Microduplication and Triplication of 22q11.2: A Highly Variable Syndrome

    Microduplication and Triplication of 22q11.2: A Highly Variable Syndrome Autor Twila M. Yobb, Martin J. Somerville, Lionel Willatt, Helen V. Firth, Karen J. Harrison, Jennifer MacKenzie, Natasha Gallo, Bernice E. Morrow, Lisa G. Shaffer, Melanie Babcock, Judy Chernos, François Bernier, Kathy Sprysak, Jesse Christiansen, Shelagh Haase, Basil G. Elyas, Margaret Lilley, Steven Bamforth, Heather E. McDermid

    Vydáno 2005
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  6. 6
    Global variation in copy number in the human genome

    Global variation in copy number in the human genome Autor Richard Redon, Shumpei Ishikawa, Karen Fitch, Lars Feuk, George H. Perry, T. Daniel Andrews, Heike Fiegler, Michael H. Shapero, Andrew R. Carson, Wei‐Wen Chen, Eun Kyung Cho, Stephanie Dallaire, Jennifer L. Freeman, Juan R. González, Mónica Gratacòs, Jing Huang, Dimitrios Rafail Kalaitzopoulos, Daisuke Komura, Jeffrey R. MacDonald, Christian R. Marshall, Rui Mei, Lyndal Montgomery, Kunihiro Nishimura, K. Okamura, Fan Shen, Martin J. Somerville, Joëlle Tchinda, Armand Valsesia, Cara Woodwark, Fengtang Yang, Junjun Zhang, Tatiana Zerjal, Jane Zhang, Lluı́s Armengol, Donald F. Conrad, Xavier Estivill, Chris Tyler‐Smith, Nigel P. Carter, Hiroyuki Aburatani, Charles Lee, Keith Jones, Stephen W. Scherer, Matthew E. Hurles

    Vydáno 2006
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  7. 7
    The clinical utility of integrative genomics in childhood cancer extends beyond targetable mutations

    The clinical utility of integrative genomics in childhood cancer extends beyond targetable mutations Autor Anita Villani, Scott Davidson, Nisha Kanwar, Winnie Lo, Yisu Li, Sarah Cohen‐Gogo, Fabio Fuligni, Lisa-Monique Edward, Nicholas Light, Mehdi Layeghifard, Ricardo Harripaul, Larissa Waldman, Bailey Gallinger, Federico Comitani, Ledia Brunga, Reid Hayes, Nathaniel D. Anderson, Arun Ramani, Kyoko E. Yuki, Sasha Blay, Brittney Johnstone, Cara Inglese, Rawan Hammad, Catherine Goudie, Andrew Y. Shuen, Jonathan D. Wasserman, Rosemarie E. Venier, Marianne Eliou, Miranda Lorenti, Carol Ann Ryan, Michael Braga, Meagan Gloven-Brown, Jianan Han, P. Montero, Famida Spatare, James A. Whitlock, Stephen W. Scherer, Kathy Chun, Martin J. Somerville, Cynthia Hawkins, Mohamed Abdelhaleem, Vijay Ramaswamy, Gino R. Somers, Lianna Kyriakopoulou, Johann Hitzler, Mary Shago, Daniel A. Morgenstern, Uri Tabori, M. Stephen Meyn, Meredith S. Irwin, David Malkin, Adam Shlien

    Vydáno 2022
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