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Evaluation of Recipients of Positive and Negative Secondary Findings Evaluations in a Hybrid CLIA-Research Sequencing Pilot.
Sapp, Julie C; Johnston, Jennifer J; Driscoll, Kate; Heidlebaugh, Alexis R; Miren Sagardia, Ane; Dogbe, D Nadine; Umstead, Kendall L; Turbitt, Erin; Alevizos, Ilias; Baron, Jeffrey; Bönnemann, Carsten; Brooks, Brian; Donkervoort, Sandra; Jee, Youn Hee; Linehan, W Marston; McMahon, Francis J; Moss, Joel; Mullikin, James C; Nielsen, Deborah; Pelayo, Eileen; Remaley, Alan T; Siegel, Richard; Su, Helen; Zarate, Carlos; Manolio, Teri A; Biesecker, Barbara B; Biesecker, Leslie G.
Afiliación
  • Sapp JC; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, Bethesda, MD 20892, USA.
  • Johnston JJ; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, Bethesda, MD 20892, USA.
  • Driscoll K; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, Bethesda, MD 20892, USA.
  • Heidlebaugh AR; Social and Behavioral Research Branch, National Human Genome Research Institute, Bethesda, MD 20892, USA.
  • Miren Sagardia A; Social and Behavioral Research Branch, National Human Genome Research Institute, Bethesda, MD 20892, USA.
  • Dogbe DN; Social and Behavioral Research Branch, National Human Genome Research Institute, Bethesda, MD 20892, USA.
  • Umstead KL; Social and Behavioral Research Branch, National Human Genome Research Institute, Bethesda, MD 20892, USA.
  • Turbitt E; Social and Behavioral Research Branch, National Human Genome Research Institute, Bethesda, MD 20892, USA.
  • Alevizos I; National Institute of Dental and Craniofacial Research, Bethesda, MD 20892, USA.
  • Baron J; Section on Growth Development, National Institute of Child Health and Human Development, Bethesda, MD 20892, USA.
  • Bönnemann C; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurologic Disorders and Stroke, Bethesda, MD 20892, USA.
  • Brooks B; Office of the Clinical Director, National Eye Institute, Bethesda, MD 20892, USA.
  • Donkervoort S; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurologic Disorders and Stroke, Bethesda, MD 20892, USA.
  • Jee YH; Section on Growth Development, National Institute of Child Health and Human Development, Bethesda, MD 20892, USA.
  • Linehan WM; Urologic Oncology Branch, National Cancer Institute, Bethesda, MD 20892, USA.
  • McMahon FJ; Human Genetics Branch, National Institutes of Mental Health, Bethesda, MD 20892, USA.
  • Moss J; Laboratory of Translational Research, National Heart, Lung, and Blood Institute, Bethesda, MD 20892, USA.
  • Mullikin JC; NIH Intramural Sequencing Center, National Human Genome Research Institute, Bethesda, MD 20892, USA.
  • Nielsen D; Urologic Oncology Branch, National Cancer Institute, Bethesda, MD 20892, USA.
  • Pelayo E; National Institute of Dental and Craniofacial Research, Bethesda, MD 20892, USA.
  • Remaley AT; Lipoprotein Metabolism Laboratory, National Heart, Lung, and Blood Institute, Bethesda, MD 20892, USA.
  • Siegel R; Office of the Clinical Director, National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, MD 20892, USA.
  • Su H; Human Immunological Diseases Section, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA.
  • Zarate C; Human Genetics Branch, National Institutes of Mental Health, Bethesda, MD 20892, USA.
  • Manolio TA; Division of Genomic Medicine, National Human Genome Research Institute, Bethesda, MD 20892, USA.
  • Biesecker BB; Social and Behavioral Research Branch, National Human Genome Research Institute, Bethesda, MD 20892, USA.
  • Biesecker LG; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, Bethesda, MD 20892, USA. Electronic address: lesb@mail.nih.gov.
Am J Hum Genet ; 103(3): 358-366, 2018 09 06.
Article en En | MEDLINE | ID: mdl-30122538

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Exoma Tipo de estudio: Diagnostic_studies / Guideline / Prognostic_studies Idioma: En Revista: Am J Hum Genet Año: 2018 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Exoma Tipo de estudio: Diagnostic_studies / Guideline / Prognostic_studies Idioma: En Revista: Am J Hum Genet Año: 2018 Tipo del documento: Article