المؤلفون: Waltz M; Department of Social Medicine, University of North Carolina, Chapel Hill, Chapel Hill, NC, USA. Electronic address: margaret_waltz@med.unc.edu., Yan H; Department of Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL, USA., Cadigan RJ; Department of Social Medicine, University of North Carolina, Chapel Hill, Chapel Hill, NC, USA., Canter C; Department of Anthropology, University of North Carolina, Chapel Hill, Chapel Hill, NC, USA., Bain L; Parent/Advocate, Knightdale, NC, USA., Bensen JT; Department of Epidemiology, University of North Carolina, Chapel Hill, Chapel Hill, NC, USA., Conway C; Parent/Advocate, Parent Advocates for Adult Children with Intellectual &/or Developmental Disabilities in NC, Chapel Hill, NC, USA., Haldeman-Englert C; Fullerton Genetics Center, Mission Health, Asheville, NC, USA., Farnan L; Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA., M Foreman AK; Department of Genetics, University of North Carolina, Chapel Hill, Chapel Hill, NC, USA., Grant TL; Department of Genetics, University of North Carolina, Chapel Hill, Chapel Hill, NC, USA., Leach B; Parent/Advocate, Family Support Program, School of Social Work, UNC Chapel Hill, Chapel Hill, NC, USA., Lin FC; Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA., Mahla M; Department of Genetics, University of North Carolina, Chapel Hill, Chapel Hill, NC, USA., O'Daniel JM; Department of Genetics, University of North Carolina, Chapel Hill, Chapel Hill, NC, USA., O'Neill SC; Department of Oncology, Georgetown University, Washington, DC, USA., Smith G; Parent/Advocate, Holly Springs, NC, USA., Powell BC; Department of Genetics, University of North Carolina, Chapel Hill, Chapel Hill, NC, USA., Berg JS; Department of Genetics, University of North Carolina, Chapel Hill, Chapel Hill, NC, USA., Rini CM; Department of Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL, USA; Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL, USA.

المصدر: Patient education and counseling [Patient Educ Couns] 2023 Apr; Vol. 109, pp. 107620. Date of Electronic Publication: 2023 Jan 02.

نوع المنشور: Randomized Controlled Trial; Journal Article; Research Support, N.I.H., Extramural

بيانات الدورية: Publisher: Elsevier Country of Publication: Ireland NLM ID: 8406280 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-5134 (Electronic) Linking ISSN: 07383991 NLM ISO Abbreviation: Patient Educ Couns

مواضيع طبية MeSH: Caregivers* , Communication*, Humans ; Child ; Physician-Patient Relations ; Surveys and Questionnaires ; Patient Participation

المؤلفون: Lee K; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA., Seifert BA; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA., Shimelis H; Mayo Clinic, Rochester, MN, USA., Ghosh R; Baylor College of Medicine, Houston, TX, USA., Crowley SB; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA., Carter NJ; GeneDx, Gaithersburg, MD, USA., Doonanco K; GeneDx, Gaithersburg, MD, USA., Foreman AK; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA., Ritter DI; Baylor College of Medicine, Houston, TX, USA., Jimenez S; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA., Trapp M; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA., Offit K; Memorial Sloan Kettering Cancer Center, New York, NY, USA., Plon SE; Baylor College of Medicine, Houston, TX, USA., Couch FJ; Mayo Clinic, Rochester, MN, USA. Couch.Fergus@mayo.edu.

المصدر: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2019 Jul; Vol. 21 (7), pp. 1497-1506. Date of Electronic Publication: 2018 Dec 03.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural

بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE

مواضيع طبية MeSH: Breast Neoplasms/*genetics , Ovarian Neoplasms/*genetics, Female ; Genetic Association Studies ; Genetic Predisposition to Disease ; Genetic Testing ; Humans

المؤلفون: Berg JS; Department of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Foreman AK; Department of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., O'Daniel JM; Department of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Booker JK; Department of Pathology and Laboratory Medicine, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Boshe L; Department of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Carey T; Department of Social Medicine, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Crooks KR; Department of Pathology and Laboratory Medicine, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Jensen BC; Division of Cardiology, Department of Medicine, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Juengst ET; Department of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.; Department of Social Medicine, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.; Center for Bioethics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Lee K; Department of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Nelson DK; Department of Social Medicine, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Powell BC; Department of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Powell CM; Division of Genetics and Metabolism, Department of Pediatrics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Roche MI; Department of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.; Department of Social Medicine, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.; Division of Genetics and Metabolism, Department of Pediatrics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Skrzynia C; Department of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Strande NT; Department of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Weck KE; Department of Pathology and Laboratory Medicine, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Wilhelmsen KC; Department of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Evans JP; Department of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

المصدر: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2016 May; Vol. 18 (5), pp. 467-75. Date of Electronic Publication: 2015 Aug 13.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural

بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Testing* , Genome, Human*, Genetic Diseases, Inborn/*diagnosis , High-Throughput Nucleotide Sequencing/*methods, Chromosome Mapping ; Genetic Diseases, Inborn/epidemiology ; Genetic Diseases, Inborn/pathology ; Genomics ; Humans ; Incidental Findings

المؤلفون: Couser NL; Department of Ophthalmology, University of North Carolina School of Medicine, Chapel Hill, North Carolina.; Department of Pediatrics, University of North Carolina School of Medicine, Chapel Hill, North Carolina.; Department of Genetics, University of North Carolina School of Medicine, Chapel Hill, North Carolina., Masood MM; University of North Carolina School of Medicine, Chapel Hill, North Carolina., Strande NT; Department of Genetics, University of North Carolina School of Medicine, Chapel Hill, North Carolina., Foreman AK; Department of Genetics, University of North Carolina School of Medicine, Chapel Hill, North Carolina., Crooks K; Department of Genetics, University of North Carolina School of Medicine, Chapel Hill, North Carolina.; Department of Pathology and Laboratory Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina., Weck KE; Department of Genetics, University of North Carolina School of Medicine, Chapel Hill, North Carolina.; Department of Pathology and Laboratory Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina., Lu M; Department of Pathology and Laboratory Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina., Wilhelmsen KC; Department of Genetics, University of North Carolina School of Medicine, Chapel Hill, North Carolina., Roche M; Department of Pediatrics, University of North Carolina School of Medicine, Chapel Hill, North Carolina.; Department of Genetics, University of North Carolina School of Medicine, Chapel Hill, North Carolina., Evans JP; Department of Genetics, University of North Carolina School of Medicine, Chapel Hill, North Carolina., Berg JS; Department of Genetics, University of North Carolina School of Medicine, Chapel Hill, North Carolina., Powell CM; Department of Pediatrics, University of North Carolina School of Medicine, Chapel Hill, North Carolina.; Department of Genetics, University of North Carolina School of Medicine, Chapel Hill, North Carolina.

المصدر: American journal of medical genetics. Part A [Am J Med Genet A] 2015 Sep; Vol. 167A (9), pp. 2176-81. Date of Electronic Publication: 2015 Apr 29.

نوع المنشور: Case Reports; Journal Article; Research Support, N.I.H., Extramural

بيانات الدورية: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

مواضيع طبية MeSH: Abnormalities, Multiple/*genetics , Muscle Hypotonia/*genetics , Seizures/*genetics, Child, Preschool ; Exome/genetics ; Humans ; Male ; Mutation, Missense/genetics ; Phenotype ; Phosphotransferases/genetics ; Syndrome

المؤلفون: Amendola LM; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA;, Dorschner MO; Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA; Department of Laboratory Medicine, University of Washington, Seattle, Washington 98195, USA; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington 98195, USA;, Robertson PD; Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA;, Salama JS; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA;, Hart R; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA;, Shirts BH; Department of Laboratory Medicine, University of Washington, Seattle, Washington 98195, USA;, Murray ML; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA; Department of Pathology, University of Washington, Seattle, Washington 98195, USA;, Tokita MJ; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA;, Gallego CJ; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA;, Kim DS; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA; Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA;, Bennett JT; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA; Department of Pediatrics, University of Washington, Seattle, Washington 98195, USA;, Crosslin DR; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA; Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA;, Ranchalis J; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA;, Jones KL; Department of Pediatrics, University of Washington, Seattle, Washington 98195, USA;, Rosenthal EA; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA;, Jarvik ER; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA;, Itsara A; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA;, Turner EH; Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA; Department of Laboratory Medicine, University of Washington, Seattle, Washington 98195, USA;, Herman DS; Department of Laboratory Medicine, University of Washington, Seattle, Washington 98195, USA;, Schleit J; Department of Pathology, University of Washington, Seattle, Washington 98195, USA;, Burt A; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA;, Jamal SM; Department of Pediatrics, Division of Genetic Medicine, University of Washington, Seattle, Washington 98195, USA;, Abrudan JL; Department of Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA; Department of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA;, Johnson AD; The Framingham Heart Study, Division of Intramural Research, National Heart, Lung and Blood Institute, Framingham, Massachusetts 01702, USA;, Conlin LK; Department of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA; Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA;, Dulik MC; Department of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA; Department of Pediatrics, Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA;, Santani A; Department of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA; Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA;, Metterville DR; Laboratory of Molecular Medicine, Partners Healthcare, Boston, Massachusetts 02115, USA;, Kelly M; Partners Healthcare Personalized Medicine, Partners Healthcare, Boston, Massachusetts 02115, USA;, Foreman AK; Department of Genetics, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA;, Lee K; Department of Genetics, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA;, Taylor KD; Translational Genomics and Population Sciences, Los Angeles Biomedical Research Institute and Department of Pediatrics at Harbor-UCLA, Torrence, California 90502, USA;, Guo X; Translational Genomics and Population Sciences, Los Angeles Biomedical Research Institute and Department of Pediatrics at Harbor-UCLA, Torrence, California 90502, USA;, Crooks K; Department of Pathology and Laboratory Medicine, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27514, USA;, Kiedrowski LA; Department of Cancer Genetics, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA;, Raffel LJ; Medical Genetics Research Institute, Cedars-Sinai Medical Center, Los Angeles, California 90048, USA;, Gordon O; Medical Genetics Research Institute, Cedars-Sinai Medical Center, Los Angeles, California 90048, USA;, Machini K; Laboratory of Molecular Medicine, Partners Healthcare, Boston, Massachusetts 02115, USA; Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA; Department of Pathology, Harvard Medical School, Boston, Massachusetts 02115, USA;, Desnick RJ; Department of Genetic and Genomic Medicine, Division of Medical Genetics, Mount Sinai Hospital, New York, New York 10029, USA;, Biesecker LG; Genetic Diseases Research Branch, National Human Genome Research Institute, Bethesda, Maryland 20892, USA;, Lubitz SA; Cardiac Arrhythmia Service and Cardiovascular Research Center, Massachusetts General Hospital, Boston, Massachusetts 02114, USA;, Mulchandani S; Department of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA;, Cooper GM; HudsonAlpha Institute for Biotechnology, Huntsville, Alabama 35806, USA;, Joffe S; Department of Medical Ethics and Health Policy, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania 19104, USA;, Richards CS; Department of Molecular and Medical Genetics, Oregon Health and Science University, Portland, Oregon 97239, USA;, Yang Y; Department of Pediatrics, Division of Infectious Disease, Los Angeles Biomedical Research Institute and Department of Pediatrics at Harbor-UCLA, Torrence, California 90502, USA;, Rotter JI; Translational Genomics and Population Sciences, Los Angeles Biomedical Research Institute and Department of Pediatrics at Harbor-UCLA, Torrence, California 90502, USA;, Rich SS; Center for Public Health Genomics, University of Virginia, Charlottesville, Virginia 22908, USA;, O'Donnell CJ; The Framingham Heart Study, Division of Intramural Research, National Heart, Lung and Blood Institute, Framingham, Massachusetts 01702, USA; Division of Cardiology, Massachusetts General Hospital, Boston, Massachusetts 02114, USA;, Berg JS; Department of Genetics, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA;, Spinner NB; Department of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA; Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA;, Evans JP; Department of Genetics, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA;, Fullerton SM; Department of Bioethics and Humanities, University of Washington, Seattle, Washington 98195, USA;, Leppig KA; Genetic Services, Group Health Cooperative, Seattle, Washington 98112, USA;, Bennett RL; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA;, Bird T; Department of Neurology, University of Washington, Seattle, Washington 98195, USA; Veterans Affairs Puget Sound Health Care System Geriatric Research, Education, and Clinical Center, Seattle, Washington 98108, USA;, Sybert VP; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA; Dermatology, Group Health Cooperative, Seattle, Washington 98112, USA;, Grady WM; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA; Department of Medicine, Division of Gastroenterology, University of Washington, Seattle, Washington 98195, USA;, Tabor HK; Department of Pediatrics, University of Washington, Seattle, Washington 98195, USA; Treuman Katz Center for Pediatric Bioethics, Seattle Children's Research Institute, Seattle, Washington 98105, USA;, Kim JH; Department of Anesthesiology and Pain Medicine, University of Washington, Seattle, Washington 98195, USA;, Bamshad MJ; Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA; Department of Pediatrics, University of Washington, Seattle, Washington 98195, USA;, Wilfond B; Treuman Katz Center for Pediatric Bioethics, Seattle Children's Research Institute, Seattle, Washington 98105, USA; Department of Pediatrics, Division of Bioethics, University of Washington, Seattle, Washington 98195, USA., Motulsky AG; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA; Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA;, Scott CR; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA; Department of Pediatrics, Division of Genetic Medicine, University of Washington, Seattle, Washington 98195, USA;, Pritchard CC; Department of Laboratory Medicine, University of Washington, Seattle, Washington 98195, USA;, Walsh TD; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA;, Burke W; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA; Department of Bioethics and Humanities, University of Washington, Seattle, Washington 98195, USA;, Raskind WH; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington 98195, USA;, Byers P; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA; Department of Pathology, University of Washington, Seattle, Washington 98195, USA;, Hisama FM; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA;, Rehm H; Laboratory of Molecular Medicine, Partners Healthcare, Boston, Massachusetts 02115, USA; Department of Pathology, Harvard Medical School, Boston, Massachusetts 02115, USA;, Nickerson DA; Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA;, Jarvik GP; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA; Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA;

المصدر: Genome research [Genome Res] 2015 Mar; Vol. 25 (3), pp. 305-15. Date of Electronic Publication: 2015 Jan 30.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Cold Spring Harbor Laboratory Press Country of Publication: United States NLM ID: 9518021 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1549-5469 (Electronic) Linking ISSN: 10889051 NLM ISO Abbreviation: Genome Res Subsets: MEDLINE

مواضيع طبية MeSH: Exome* , Genomics*/methods , Incidental Findings*, Adult ; Black People/genetics ; Female ; Gene Frequency ; Genes, Dominant ; Genetic Association Studies ; Genetic Testing ; Genome, Human ; High-Throughput Nucleotide Sequencing ; Humans ; Male ; Phenotype ; Polymorphism, Single Nucleotide ; White People/genetics

المؤلفون: Foreman AK; Department of Genetics, School of Medicine, University of North Carolina at Chapel Hill, CB 7264, Chapel Hill, NC 27599, USA. jpevans@med.unc.edu., Lee K, Evans JP

المصدر: North Carolina medical journal [N C Med J] 2013 Nov-Dec; Vol. 74 (6), pp. 500-4.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Medical Society Of The State Of North Carolina Country of Publication: United States NLM ID: 2984805R Publication Model: Print Cited Medium: Print ISSN: 0029-2559 (Print) Linking ISSN: 00292559 NLM ISO Abbreviation: N C Med J Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Services* , Sequence Analysis*/instrumentation , Sequence Analysis*/methods, Humans ; North Carolina