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Universal Germline Genetic Testing for Hereditary Cancer Syndromes in Patients With Solid Tumor Cancer.
Esplin, Edward D; Nielsen, Sarah M; Bristow, Sara L; Garber, Judy E; Hampel, Heather; Rana, Huma Q; Samadder, N Jewel; Shore, Neal D; Nussbaum, Robert L.
Afiliación
  • Esplin ED; Invitae, San Francisco, CA.
  • Nielsen SM; Invitae, San Francisco, CA.
  • Bristow SL; Invitae, San Francisco, CA.
  • Garber JE; Dana Farber Cancer Institute, Boston, MA.
  • Hampel H; Division of Clinical Cancer Genomics, Department of Medical Oncology & Therapeutic Research, City of Hope National Cancer Center, Duarte, CA.
  • Rana HQ; Dana Farber Cancer Institute, Boston, MA.
  • Samadder NJ; Center for Individualized Medicine, Mayo Clinic, Phoenix, AZ.
  • Shore ND; Division of Gastroenterology and Hepatology, Department of Medicine, Mayo Clinic, Phoenix, AZ.
  • Nussbaum RL; Department of Clinical Genomics, Mayo Clinic, Phoenix, AZ.
JCO Precis Oncol ; 6: e2100516, 2022 09.
Article en En | MEDLINE | ID: mdl-36108258
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Síndromes Neoplásicos Hereditarios Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: JCO Precis Oncol Año: 2022 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Síndromes Neoplásicos Hereditarios Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: JCO Precis Oncol Año: 2022 Tipo del documento: Article