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Impact of Variant Reclassification in Cancer Predisposition Genes on Clinical Care.
Chiang, Jianbang; Chia, Tze Hao; Yuen, Jeanette; Shaw, Tarryn; Li, Shao-Tzu; Binte Ishak, Nur Diana; Chew, Ee Ling; Chong, Siao Ting; Chan, Sock Hoai; Ngeow, Joanne.
Afiliação
  • Chiang J; Cancer Genetics Service, Division of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore.
  • Chia TH; Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore, Singapore.
  • Yuen J; Cancer Genetics Service, Division of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore.
  • Shaw T; Cancer Genetics Service, Division of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore.
  • Li ST; Cancer Genetics Service, Division of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore.
  • Binte Ishak ND; Cancer Genetics Service, Division of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore.
  • Chew EL; Cancer Genetics Service, Division of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore.
  • Chong ST; Cancer Genetics Service, Division of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore.
  • Chan SH; Cancer Genetics Service, Division of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore.
  • Ngeow J; Cancer Genetics Service, Division of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore.
JCO Precis Oncol ; 5: 577-584, 2021 11.
Article em En | MEDLINE | ID: mdl-34994607

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Síndromes Neoplásicas Hereditárias / Testes Genéticos / Predisposição Genética para Doença Tipo de estudo: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: JCO Precis Oncol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Singapura

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Síndromes Neoplásicas Hereditárias / Testes Genéticos / Predisposição Genética para Doença Tipo de estudo: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: JCO Precis Oncol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Singapura