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The NIH Undiagnosed Diseases Program and Network: Applications to modern medicine.
Gahl, William A; Mulvihill, John J; Toro, Camilo; Markello, Thomas C; Wise, Anastasia L; Ramoni, Rachel B; Adams, David R; Tifft, Cynthia J.
Afiliación
  • Gahl WA; NIH Undiagnosed Diseases Network, Common Fund, Office of the Director and the National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, United States.
  • Mulvihill JJ; NIH Undiagnosed Diseases Network, Common Fund, Office of the Director and the National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, United States; Department of Pediatrics, University of Oklahoma, Oklahoma City, OK, United States. Electronic address: John.Mulvihill@n
  • Toro C; NIH Undiagnosed Diseases Network, Common Fund, Office of the Director and the National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, United States.
  • Markello TC; NIH Undiagnosed Diseases Network, Common Fund, Office of the Director and the National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, United States.
  • Wise AL; NIH Undiagnosed Diseases Network, Common Fund, Office of the Director and the National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, United States.
  • Ramoni RB; Department for Biomedical Informatics, Harvard Medical School, Department of Oral Health Policy and Epidemiology, Harvard Dental School, Cambridge, MA, United States.
  • Adams DR; NIH Undiagnosed Diseases Network, Common Fund, Office of the Director and the National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, United States.
  • Tifft CJ; NIH Undiagnosed Diseases Network, Common Fund, Office of the Director and the National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, United States.
Mol Genet Metab ; 117(4): 393-400, 2016 Apr.
Article en En | MEDLINE | ID: mdl-26846157
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Investigación / Enfermedades Raras / Medicina de Precisión / National Institutes of Health (U.S.) Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: Mol Genet Metab Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Investigación / Enfermedades Raras / Medicina de Precisión / National Institutes of Health (U.S.) Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: Mol Genet Metab Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos