Breast cancer susceptibility variants alter risks in familial disease

Journal of Medical Genetics

Volumn 47, Issue 2, 2010, Pages 126-131

  Latif, Ayse ^a   Hadfield, Kristen D ^a   Roberts, Stephen A ^a   Shenton, Andrew ^a   Lalloo, Fiona ^a   Black, Graeme C M ^a   Howell, Anthony ^b   Evans, D Gareth ^a,b   Newman, William G ^a  

^a UNIVERSITY OF MANCHESTER   (United Kingdom)

^b WYTHENSHAWE HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; BREAST CANCER; CANCER RISK; CANCER SUSCEPTIBILITY; CASP8 GENE; CHROMOSOME 8Q; CONTROLLED STUDY; FAMILIAL CANCER; FEMALE; FGFR2 GENE; GENE; GENE FREQUENCY; GENE MUTATION; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MAP3K1 GENE; NUCLEOTIDE SEQUENCE; ONCOGENE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; TOX3 GENE;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; BREAST NEOPLASMS; CASPASE 8; CHI-SQUARE DISTRIBUTION; COHORT STUDIES; FEMALE; GENES, BRCA1; GENES, BRCA2; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; MAP KINASE KINASE KINASE 1; MICROFILAMENT PROTEINS; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 2; RISK ASSESSMENT;

EID: 77349114728     PISSN: 00222593     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2009.067256     Document Type: Article

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