SEOM clinical guidelines for hereditary cancer
Clin. transl. oncol. (Print)
; 13(8): 580-586, ago. 2011. tab, ilus
Article
in English
| IBECS
| ID: ibc-125860
Responsible library:
ES1.1
Localization: BNCS
ABSTRACT
Research in genetics has facilitated the identification of highly penetrant genes responsible for a large number of diseases. In the oncology field, genetic counselling and gene testing are focused on the two most common syndromes in familial cancer hereditary breast and ovarian cancer syndrome (HBOC) and hereditary non-polyposis colorectal cancer or Lynch syndrome (LS). The objective of this guideline in hereditary cancer is to summarise the current state of knowledge and make recommendations in the areas of diagnosis, prevention and treatment of hereditary cancer (AU)
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Collection:
National databases
/
Spain
Database:
IBECS
Main subject:
Biomarkers, Tumor
/
Medical Oncology
/
Neoplasms
Type of study:
Diagnostic study
/
Practice guideline
/
Prognostic study
Limits:
Adult
/
Female
/
Humans
/
Male
Language:
English
Journal:
Clin. transl. oncol. (Print)
Year:
2011
Document type:
Article
Institution/Affiliation country:
Catalan Institut of Oncology (ICO)/Spain
/
General Yagüe Hospital/Spain
/
Hospital Lozano Blesa/Spain
/
Vall d'Hebron Institute of Oncology (VHIO)/Spain
/
Valles Institute of Oncology/Spain