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Novel and recurrent BRCA1/BRCA2 mutations in early onset and familial breast and ovarian cancer detected in the Program of Genetic Counseling in Cancer of Valencian Community (eastern Spain). Relationship of family phenotypes with mutation prevalence

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Year: 2013
Type: article
Study design: Observational Study
Source: Familial Cancer
DOI: 10.1007/s10689-013-9622-2
Authors: Inmaculada de Juan Jiménez, Zaida García Casado, Sarai Palanca Suela, Eva Esteban Cardeñosa, José Antonio López Guerrero, Ángel Segura Huerta, Isabel Chirivella González, Ana Beatriz Sánchez Heras, Mª José Juan Fita, Isabel Tena García, Carmen Guillen Ponce, Eduardo Martínez de Dueñas, Ignacio Romero Noguera, Dolores Salas Trejo, Mercedes Goicoechea Sáez, Pascual Bolufer Gilabert
Institutions: Hospital Universitari i Politècnic La Fe, Fundación Instituto Valenciano de Oncología, Hospital Clínico Universitario de Valencia, Hospital General Universitario de Elche, Hospital General Universitari de Castelló, Conselleria de Sanitat Universal i Salut Pública
Language: English

Topic: BRCA gene mutations in cancer
Subfield: Genetics
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed
OpenAlex ID: W2055294836
FWCI: 1.544
Cites: 37
Cited by: 35
Related to: 10
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