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The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease.
Ramoni, Rachel B; Mulvihill, John J; Adams, David R; Allard, Patrick; Ashley, Euan A; Bernstein, Jonathan A; Gahl, William A; Hamid, Rizwan; Loscalzo, Joseph; McCray, Alexa T; Shashi, Vandana; Tifft, Cynthia J; Wise, Anastasia L.
Afiliación
  • Ramoni RB; Department of Biomedical Informatics, Harvard Medical School, Boston, MA 02115, USA; Department of Epidemiology and Health Promotion, New York University College of Dentistry, New York, NY 10010, USA. Electronic address: rachelramoni@nyu.edu.
  • Mulvihill JJ; National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA.
  • Adams DR; National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA.
  • Allard P; Institute for Society and Genetics, University of California, Los Angeles, Los Angeles, CA 90095, USA; Department of Environmental Health Sciences, Fielding School of Public Health, University of California, Los Angeles, Los Angeles, CA 90095 USA.
  • Ashley EA; Departments of Medicine and Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Bernstein JA; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Gahl WA; National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA.
  • Hamid R; Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
  • Loscalzo J; Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.
  • McCray AT; Department of Biomedical Informatics, Harvard Medical School, Boston, MA 02115, USA.
  • Shashi V; Department of Pediatrics, Duke University School of Medicine, Durham, NC 27707, USA.
  • Tifft CJ; National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA.
  • Wise AL; National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA.
Am J Hum Genet ; 100(2): 185-192, 2017 02 02.
Article en En | MEDLINE | ID: mdl-28157539
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedades Raras Tipo de estudio: Guideline / Prognostic_studies País/Región como asunto: America do norte Idioma: En Revista: Am J Hum Genet Año: 2017 Tipo del documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedades Raras Tipo de estudio: Guideline / Prognostic_studies País/Región como asunto: America do norte Idioma: En Revista: Am J Hum Genet Año: 2017 Tipo del documento: Article