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Stakeholder perspectives on the implementation of genetic carrier screening in a changing landscape.
Holtkamp, Kim C A; Vos, Evelien M; Rigter, Tessel; Lakeman, Phillis; Henneman, Lidewij; Cornel, Martina C.
Afiliação
  • Holtkamp KC; Department of Clinical Genetics, Section of Community Genetics, Amsterdam Public Health Research Institute, VU University Medical Center, PO Box 7057 (BS7 A-509), 1007 MB, Amsterdam, The Netherlands. k.holtkamp@vumc.nl.
  • Vos EM; Department of Clinical Genetics, Section of Community Genetics, Amsterdam Public Health Research Institute, VU University Medical Center, PO Box 7057 (BS7 A-509), 1007 MB, Amsterdam, The Netherlands.
  • Rigter T; Department of Clinical Genetics, Section of Community Genetics, Amsterdam Public Health Research Institute, VU University Medical Center, PO Box 7057 (BS7 A-509), 1007 MB, Amsterdam, The Netherlands.
  • Lakeman P; Department of Clinical Genetics, Academic Medical Center, Amsterdam, The Netherlands.
  • Henneman L; Department of Clinical Genetics, Section of Community Genetics, Amsterdam Public Health Research Institute, VU University Medical Center, PO Box 7057 (BS7 A-509), 1007 MB, Amsterdam, The Netherlands.
  • Cornel MC; Department of Clinical Genetics, Section of Community Genetics, Amsterdam Public Health Research Institute, VU University Medical Center, PO Box 7057 (BS7 A-509), 1007 MB, Amsterdam, The Netherlands.
BMC Health Serv Res ; 17(1): 146, 2017 02 16.
Article em En | MEDLINE | ID: mdl-28209157
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Testes Genéticos / Doenças Genéticas Inatas / Heterozigoto Tipo de estudo: Diagnostic_studies / Guideline / Qualitative_research / Screening_studies Limite: Humans País/Região como assunto: Europa Idioma: En Revista: BMC Health Serv Res Assunto da revista: PESQUISA EM SERVICOS DE SAUDE Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Holanda
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Testes Genéticos / Doenças Genéticas Inatas / Heterozigoto Tipo de estudo: Diagnostic_studies / Guideline / Qualitative_research / Screening_studies Limite: Humans País/Região como assunto: Europa Idioma: En Revista: BMC Health Serv Res Assunto da revista: PESQUISA EM SERVICOS DE SAUDE Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Holanda