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Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data.
Jenkins, Mary M; Almli, Lynn M; Pangilinan, Faith; Chong, Jessica X; Blue, Elizabeth E; Shapira, Stuart K; White, Janson; McGoldrick, Daniel; Smith, Joshua D; Mullikin, James C; Bean, Christopher J; Nembhard, Wendy N; Lou, Xiang-Yang; Shaw, Gary M; Romitti, Paul A; Keppler-Noreuil, Kim; Yazdy, Mahsa M; Kay, Denise M; Carter, Tonia C; Olshan, Andrew F; Moore, Kristin J; Nascone-Yoder, Nanette; Finnell, Richard H; Lupo, Philip J; Feldkamp, Marcia L; Nickerson, Deborah A; Bamshad, Michael J; Brody, Lawrence C; Reefhuis, Jennita.
  • Jenkins MM; National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Almli LM; National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Pangilinan F; Carter Consulting Incorporated, Atlanta, Georgia.
  • Chong JX; National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.
  • Blue EE; Department of Pediatrics, University of Washington, Seattle, Washington.
  • Shapira SK; Department of Medicine, University of Washington, Seattle, Washington.
  • White J; National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • McGoldrick D; Department of Pediatrics, University of Washington, Seattle, Washington.
  • Smith JD; Department of Genome Sciences, University of Washington, Seattle, Washington.
  • Mullikin JC; Department of Genome Sciences, University of Washington, Seattle, Washington.
  • Bean CJ; National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.
  • Nembhard WN; National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Lou XY; Fay W Boozman College of Public Health, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
  • Shaw GM; College of Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
  • Romitti PA; Stanford University School of Medicine, Department of Pediatrics, Stanford, California.
  • Keppler-Noreuil K; Department of Epidemiology, University of Iowa, Iowa City, Iowa.
  • Yazdy MM; Children's National Medical Center, George Washington University, Washington, District of Columbia.
  • Kay DM; Massachusetts Department of Public Health, Boston, Massachusetts.
  • Carter TC; Division of Genetics, Wadsworth Center, New York State Department of Health, Albany, New York.
  • Olshan AF; Marshfield Clinic Research Institute, Marshfield, Wisconsin.
  • Moore KJ; Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, North Carolina.
  • Nascone-Yoder N; Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, North Carolina.
  • Finnell RH; Department of Molecular Biomedical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina.
  • Lupo PJ; Center for Precision Environmental Health, Departments of Molecular & Cellular Biology and Medicine, Baylor College of Medicine, Houston, Texas.
  • Feldkamp ML; Department of Pediatrics, Section of Hematology-Oncology, Baylor College of Medicine, Houston, Texas.
  • Nickerson DA; University of Washington, Seattle, Washington.
  • Bamshad MJ; Department of Genome Sciences, University of Washington, Seattle, Washington.
  • Brody LC; Department of Pediatrics, University of Washington, Seattle, Washington.
  • Reefhuis J; Department of Genome Sciences, University of Washington, Seattle, Washington.
Birth Defects Res ; 111(20): 1618-1632, 2019 12 01.
Article en En | MEDLINE | ID: mdl-31328417
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Anomalías Congénitas / Interacción Gen-Ambiente / Secuenciación del Exoma Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2019 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Anomalías Congénitas / Interacción Gen-Ambiente / Secuenciación del Exoma Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2019 Tipo del documento: Article