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Barriers to completion of cascade genetic testing: how can we improve the uptake of testing for hereditary breast and ovarian cancer syndrome?
Kahn, Ryan Matthew; Ahsan, Muhammad Danyal; Chapman-Davis, Eloise; Holcomb, Kevin; Nitecki, Roni; Rauh-Hain, Jose Alejandro; Fowlkes, Rana Khan; Tubito, Francesca; Pires, Maira; Christos, Paul J; Tkachuk, Kaitlyn; Krinsky, Hannah; Sharaf, Ravi N; Offit, Kenneth; Lipkin, Steven; Frey, Melissa K.
Afiliação
  • Kahn RM; Dept. of Obstetrics and Gynecology, Weill Cornell Medicine, 525 E 68th St., J-130, 10065, New York, NY, USA. KahnR@mskcc.org.
  • Ahsan MD; Dept. of Gynecologic Oncology, Weill Cornell Medicine, New York, NY, USA.
  • Chapman-Davis E; Dept. of Gynecologic Oncology, Weill Cornell Medicine, New York, NY, USA.
  • Holcomb K; Dept. of Gynecologic Oncology, Weill Cornell Medicine, New York, NY, USA.
  • Nitecki R; Dept. of Gynecologic Oncology, MD Anderson Cancer Center, Houston, TX, USA.
  • Rauh-Hain JA; Dept. of Gynecologic Oncology, MD Anderson Cancer Center, Houston, TX, USA.
  • Fowlkes RK; Dept. of Obstetrics and Gynecology, Weill Cornell Medicine, 525 E 68th St., J-130, 10065, New York, NY, USA.
  • Tubito F; Genetic Counseling, Weill Cornell Medicine, New York, NY, USA.
  • Pires M; Genetic Counseling, Weill Cornell Medicine, New York, NY, USA.
  • Christos PJ; Department of Population Health Sciences, Weill Cornell Medicine, New York, NY, USA.
  • Tkachuk K; Dept. of Clinical Genetics Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Krinsky H; Dept. of Obstetrics and Gynecology, Weill Cornell Medicine, 525 E 68th St., J-130, 10065, New York, NY, USA.
  • Sharaf RN; Dept. of Gastroenterology, Weill Cornell Medicine, New York, NY, USA.
  • Offit K; Dept. of Clinical Genetics Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Lipkin S; Genetic Counseling, Weill Cornell Medicine, New York, NY, USA.
  • Frey MK; Dept. of Gynecologic Oncology, Weill Cornell Medicine, New York, NY, USA.
Fam Cancer ; 22(2): 127-133, 2023 04.
Article em En | MEDLINE | ID: mdl-36207653
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Neoplasias da Mama / Síndrome Hereditária de Câncer de Mama e Ovário Tipo de estudo: Observational_studies / Prognostic_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Neoplasias da Mama / Síndrome Hereditária de Câncer de Mama e Ovário Tipo de estudo: Observational_studies / Prognostic_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article