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Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study.
Peter, Michelle; Hammond, Jennifer; Sanderson, Saskia C; Gurasashvili, Jana; Hunter, Amy; Searle, Beverly; Patch, Christine; Chitty, Lyn S; Hill, Melissa; Lewis, Celine.
Afiliação
  • Peter M; NHS North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK. michelle.lowe@gosh.nhs.uk.
  • Hammond J; Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, UK. michelle.lowe@gosh.nhs.uk.
  • Sanderson SC; NHS North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Gurasashvili J; Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, UK.
  • Hunter A; NHS North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Searle B; Our Future Health, London, UK.
  • Patch C; NHS North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Chitty LS; Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, UK.
  • Hill M; Genetic Alliance UK, London, UK.
  • Lewis C; Unique - Rare Chromosome Disorder Support Group, Oxted, UK.
Eur J Hum Genet ; 30(5): 604-610, 2022 05.
Article em En | MEDLINE | ID: mdl-35264738
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pais / Doenças Raras Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pais / Doenças Raras Idioma: En Ano de publicação: 2022 Tipo de documento: Article