Resultats de la cerca - Kerry K. Brown

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  1. 1
    American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants

    American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants per Hutton M. Kearney, Erik C. Thorland, Kerry K. Brown, Fabiola Quintero‐Rivera, Sarah T. South

    Publicat 2011
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  2. 2
    ACMG clinical laboratory standards for next-generation sequencing

    ACMG clinical laboratory standards for next-generation sequencing per Heidi L. Rehm, Sherri J. Bale, Pınar Bayrak‐Toydemir, Jonathan S. Berg, Kerry K. Brown, Joshua L. Deignan, Michael J. Friez, Birgit Funke, Madhuri Hegde, Elaine Lyon

    Publicat 2013
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  3. 3
    <scp><i>HOXA</i></scp><i>2</i>Haploinsufficiency in Dominant Bilateral Microtia and Hearing Loss

    <scp><i>HOXA</i></scp><i>2</i>Haploinsufficiency in Dominant Bilateral Microtia and Hearing Loss per Kerry K. Brown, Lucas Moura Viana, Cecilia C. Helwig, Maria A. Artunduaga, Lourdes Quintanilla‐Dieck, Patricia Jarrin, Gabriel Osorno, Barbara McDonough, Steven R. DePalma, Roland D. Eavey, Jonathan G. Seidman, Christine E. Seidman

    Publicat 2013
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  4. 4
    Characterization of Apparently Balanced Chromosomal Rearrangements from the Developmental Genome Anatomy Project

    Characterization of Apparently Balanced Chromosomal Rearrangements from the Developmental Genome Anatomy Project per Anne W. Higgins, Fowzan S. Alkuraya, Amy F. Bosco, Kerry K. Brown, G.A.P. Bruns, Diana Donovan, R.E. Eisenman, Yanli Fan, Chantal G. Farra, Heather Ferguson, James F. Gusella, David J. Harris, Steven R. Herrick, Chantal Kelly, Hyung Goo Kim, Shotaro Kishikawa, Bruce R. Korf, Shashikant Kulkarni, Eric Lally, Natalia T. Leach, Emma Lemyre, Janine Lewis, Azra H. Ligon, Lu W, Richard L. Maas, Marcy E. MacDonald, Steven D.P. Moore, Roxanna E. Peters, Bradley J. Quade, Fabiola Quintero‐Rivera, Irfan Saadi, Yiping Shen, Jay Shendure, Robin E. Williamson, Cynthia C. Morton

    Publicat 2008
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  5. 5
    De novo mutations in histone-modifying genes in congenital heart disease

    De novo mutations in histone-modifying genes in congenital heart disease per Samir Zaidi, Murim Choi, Hiroko Wakimoto, Lijiang Ma, Jianming Jiang, John D. Overton, Angela Romano-Adesman, Robert Bjornson, Roger E. Breitbart, Kerry K. Brown, Nicholas Carriero, Yee Him Cheung, John Deanfield, Steven R. DePalma, Khalid A. Fakhro, Joseph Glessner, Hákon Hákonarson, Michael J. Italia, Jonathan R. Kaltman, Juan Pablo Kaski, Richard Kim, Jennie Kline, Teresa Lee, Jeremy Leipzig, Alexander Lopez, Shrikant Mane, Laura E. Mitchell, Jane W. Newburger, Michael Parfenov, Itsik Pe’er, George A. Porter, Amy E. Roberts, Ravi Sachidanandam, Stephan Sanders, Howard Seiden, Matthew W. State, Sai Lakshmi Subramanian, Irina R. Tikhonova, Wei Wang, Dorothy Warburton, Peter S. White, Ismée A. Williams, Hongyu Zhao, Jonathan G. Seidman, Martina Brueckner, Wendy K. Chung, Bruce D. Gelb, Elizabeth Goldmuntz, Christine E. Seidman, Richard P. Lifton

    Publicat 2013
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