Molecular characterization and cancer risk associated with BRCA1 and BRCA2 splice site variants identified in multiple-case breast cancer families.

Human mutation

Volumn 26, Issue 5, 2005, Pages 495-

  Tesoriero, A A ^a   Wong, E M ^a   Jenkins, M A ^a   Hopper, J L ^a   Brown, M A ^a   Chenevix Trench, G ^a   Spurdle, A B ^a   Southey, M C ^a  

^a UNIVERSITY OF MELBOURNE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

MESSENGER RNA;

ALTERNATIVE RNA SPLICING; ARTICLE; BREAST TUMOR; FAMILY HEALTH; FEMALE; GENETIC VARIABILITY; GENETICS; HUMAN; METABOLISM; OVARY TUMOR; RISK FACTOR; RNA SPLICING; STATISTICAL ANALYSIS; TUMOR SUPPRESSOR GENE;

ALTERNATIVE SPLICING; BREAST NEOPLASMS; DATA INTERPRETATION, STATISTICAL; FAMILY HEALTH; FEMALE; GENES, BRCA1; GENES, BRCA2; HUMANS; OVARIAN NEOPLASMS; RISK FACTORS; RNA SPLICE SITES; RNA, MESSENGER; VARIATION (GENETICS);

EID: 33644529562     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9379     Document Type: Article

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