Novel and recurrentBRCA1/BRCA2mutations 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
✍ Scribed by Juan Jiménez, Inmaculada; GarcÃa Casado, Zaida; Palanca Suela, Sarai; Esteban Cardeñosa, Eva; López Guerrero, José Antonio; Segura Huerta, Ãngel; Chirivella González, Isabel; Sánchez Heras, Ana Beatriz; Juan Fita, Mª José; Tena GarcÃa, Isabel; Guillen Ponce, Carmen; MartÃnez de Dueñas, Eduardo; Romero Noguera, Ignacio; Salas Trejo, Dolores; Goicoechea Sáez, Mercedes; Bolufer Gilabert, Pascual
- Book ID
- 120253480
- Publisher
- Springer Netherlands
- Year
- 2013
- Tongue
- English
- Weight
- 304 KB
- Volume
- 12
- Category
- Article
- ISSN
- 1389-9600
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📜 SIMILAR VOLUMES
The presence of genomic rearrangements of the BRCA1 gene in breast and/or ovarian cancer families has been intensively investigated in patients from various countries over the last years. A number of different rearrangements have been reported by several studies that clearly document the involvement