Mendelian genetics of rare-and not so rare-cancers

Mendelian genetics forms the basis for gene‐informed risk assessment and management for the patient and family, and should be at the very foundation of 21st century personalization of healthcare. Yet this is an underutilized commodity. Identification and characterization of germline mutations in the...

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Veröffentlicht in:	Annals of the New York Academy of Sciences 2010-12, Vol.1214 (1), p.70-82
1. Verfasser:	Eng, Charis
Format:	Artikel
Sprache:	eng
Schlagworte:	Genetic Counseling Genetics Germ-Line Mutation Humans molecular diagnostics multiple endocrine neoplasia syndromes Mutation Neoplastic Syndromes, Hereditary - diagnosis Neoplastic Syndromes, Hereditary - genetics Neoplastic Syndromes, Hereditary - prevention & control personalized healthcare predictive testing Proto-Oncogene Proteins - genetics Proto-Oncogene Proteins - metabolism PTEN hamartoma tumor syndrome SDH-related pheochromocytoma/paraganglioma Thyroid cancer
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