Your browser doesn't support javascript.
loading
The Meaning of Informed Consent: Genome Editing Clinical Trials for Sickle Cell Disease.
Desine, Stacy; Hollister, Brittany M; Abdallah, Khadijah E; Persaud, Anitra; Hull, Sara Chandros; Bonham, Vence L.
Afiliação
  • Desine S; Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
  • Hollister BM; Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
  • Abdallah KE; Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
  • Persaud A; Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
  • Hull SC; Department of Bioethics, Clinical Center, National Institutes of Health, Bethesda, Maryland, USA.
  • Bonham VL; Bioethics Core, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
AJOB Empir Bioeth ; 11(4): 195-207, 2020.
Article em En | MEDLINE | ID: mdl-33044907
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Terapia Genética / Acesso à Informação / Edição de Genes / Consentimento Livre e Esclarecido / Anemia Falciforme Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Terapia Genética / Acesso à Informação / Edição de Genes / Consentimento Livre e Esclarecido / Anemia Falciforme Idioma: En Ano de publicação: 2020 Tipo de documento: Article