Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing.

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Title: Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing.
Authors: Reuter CM; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA., Kohler JN; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA., Bonner D; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA., Zastrow D; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA., Fernandez L; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA., Dries A; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA., Marwaha S; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA., Davidson J; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA., Brokamp E; Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN., Herzog M; Department of Human Genetics, University of California Los Angeles, Los Angeles, CA., Hong J; Department of Medicine, Brigham and Women's Hospital, Boston, MA., Macnamara E; Undiagnosed Diseases Program, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD., Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX., Schoch K; Department of Pediatrics, Duke University Medical Center, Durham, NC., Spillmann R; Department of Pediatrics, Duke University Medical Center, Durham, NC., Loscalzo J; Department of Medicine, Brigham and Women's Hospital, Boston, MA., Krier J; Department of Medicine, Brigham and Women's Hospital, Boston, MA., Stoler J; Division of Genetics, Boston Children's Hospital, Boston, MA., Sweetser D; Division of Medical Genetics and Metabolism, Department of Pediatrics, Massachusetts General Hospital, Boston, MA., Palmer CGS; Department of Human Genetics, University of California Los Angeles, Los Angeles, CA.; Psychiatry & Biobehavioral Sciences, University of California Los Angeles, Los Angeles, CA.; Institute for Society & Genetics, University of California Los Angeles, Los Angeles, CA., Phillips JA; Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN., Shashi V; Department of Pediatrics, Duke University Medical Center, Durham, NC., Adams DA; Undiagnosed Diseases Program, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD., Yang Y; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX., Ashley EA; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA.; Department of Genetics, Stanford University School of Medicine, Stanford, CA., Fisher PG; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, CA.; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA., Mulvihill JJ; Division of Genomic Medicine, National Human Genome Research Institute, Bethesda, MD., Bernstein JA; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA., Wheeler MT; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA.
Corporate Authors: Undiagnosed Diseases Network
Source: Journal of genetic counseling [J Genet Couns] 2019 Dec; Vol. 28 (6), pp. 1107-1118. Date of Electronic Publication: 2019 Sep 03.
Publication Type: Journal Article; Research Support, N.I.H., Extramural
Journal Info: Publisher: Wiley Country of Publication: United States NLM ID: 9206865 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-3599 (Electronic) Linking ISSN: 10597700 NLM ISO Abbreviation: J Genet Couns Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1573-3599
DOI:10.1002/jgc4.1161