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Is there a way to reduce the inequity in variant interpretation on the basis of ancestry?
Appelbaum, Paul S; Burke, Wylie; Parens, Erik; Zeevi, David A; Arbour, Laura; Garrison, Nanibaa' A; Bonham, Vence L; Chung, Wendy K.
Afiliação
  • Appelbaum PS; Department of Psychiatry, Columbia University Irving Medical Center, and New York State Psychiatric Institute, New York, NY 10032, USA. Electronic address: psa21@columbia.edu.
  • Burke W; Department of Bioethics and Humanities, University of Washington, Seattle, WA 98195, USA.
  • Parens E; The Hastings Center, Garrison, NY 10524, USA.
  • Zeevi DA; Dor Yeshorim, The Committee for the Prevention of Jewish Genetic Diseases, Jerusalem, Israel.
  • Arbour L; Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada; Division of Medical Sciences, University of Victoria, Victoria, BC V8P 5C2, Canada; BC Children's Hospital Research Institute, Victoria, BC V8P 5C2, Canada.
  • Garrison NA; Institute for Society and Genetics, University of California, Los Angeles, Los Angeles, CA 90095, USA; Institute for Precision Health, University of California Los Angeles, Los Angeles, CA 90095; Division of General Internal Medicine and Health Services Research, University of California, Los Angele
  • Bonham VL; Social and Behavioral Research Branch, National Human Genome Research Institute, Bethesda, MD 20892, USA.
  • Chung WK; Department of Pediatrics, Columbia University Irving Medical Center, New York, NY 10032, USA; Department of Medicine, Columbia University Irving Medical Center, New York, NY 10032, USA.
Am J Hum Genet ; 109(6): 981-988, 2022 06 02.
Article em En | MEDLINE | ID: mdl-35659933
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Etnicidade / Testes Genéticos Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans País/Região como assunto: America do norte Idioma: En Revista: Am J Hum Genet Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Etnicidade / Testes Genéticos Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans País/Região como assunto: America do norte Idioma: En Revista: Am J Hum Genet Ano de publicação: 2022 Tipo de documento: Article