Should genes for non-syndromic hearing loss be included in reproductive genetic carrier screening: Views of people with a personal or family experience of deafness.

Freeman, Lucinda; Bristowe, Lisa; Kirk, Edwin P; Delatycki, Martin B; Scully, Jackie Leach

Freeman, Lucinda; Bristowe, Lisa; Kirk, Edwin P; Delatycki, Martin B; Scully, Jackie Leach.

Afiliação

Freeman L; School of Women's and Children's Health, University of New South Wales, Randwick, New South Wales, Australia.
Bristowe L; Graduate School of Health, University of Technology Sydney, Sydney, New South Wales, Australia.
Kirk EP; Centre for Clinical Genetics, Sydney Children's Hospitals Network, Sydney, New South Wales, Australia.
Delatycki MB; School of Women's and Children's Health, University of New South Wales, Randwick, New South Wales, Australia.
Scully JL; Centre for Clinical Genetics, Sydney Children's Hospitals Network, Sydney, New South Wales, Australia.

J Genet Couns ; 2023 Aug 02.

Article em En | MEDLINE | ID: mdl-37533186

Palavras-chave

attitudes; deafness; genetic testing; lived experience; reproductive carrier screening; stakeholder views

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Idioma: En Revista: J Genet Couns Assunto da revista: GENETICA MEDICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Austrália País de publicação: Estados Unidos

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