Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics
Sarah S. KaliaDivision of Genetics, Brigham and Women's Hospital, Boston, Massachusetts, USAKathy AdelmanPatient advocate, Livermore, California, USASherri J. BaleWendy K. ChungDepartment of Medicine, Columbia University, New York, New York, USAChristine M. EngDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USAJames P. EvansDepartment of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USAGail E. HermanInstitute for Genomic Medicine, Nationwide Children's Hospital and Department of Pediatrics, The Ohio State University, Columbus, Ohio, USASophia B. HufnagelDivision of Genetics and Metabolism, Children's National Health System, Washington, DC, USATeri E. KleinDepartment of Genetics, Stanford University School of Medicine, Palo Alto, California, USABruce R. KorfDepartment of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USAKent D. McKelveyDepartment of Family Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USAKelly E. OrmondDepartment of Genetics, Stanford University School of Medicine, Palo Alto, California, USAC. Sue RichardsDepartment of Molecular and Medical Genetics, Oregon Health & Science University, Portland, Oregon, USAChristopher N. VlangosDepartment of Pathology, Virginia Commonwealth University School of Medicine, Richmond, Virginia, USAMichael S. WatsonAmerican College of Medical Genetics and Genomics, Bethesda, Maryland, USAChrista Lese MartinAutism & Developmental Medicine Institute, Geisinger Health System, Lewisburg, Pennsylvania, USADavid T. MillerDivision of Genetics and Genomics, Boston Children's Hospital, Boston, Massachusetts, USA
2016en
ABI
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