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Journal of Medical Genetics|February 4, 2005
Classification of BRCA1 missense variants of unknown clinical significanceC M Phelan, V Dapic, B Tice, et al.
Oral Oncology|May 10, 2005
Association between polymorphisms of the GPX1 gene and second primary tumours after index squamous cell cancer of the head and neckS Jefferies, Z Kote-Jarai, D Goldgar, et al.
American Journal of Human Genetics|April 29, 1998
Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage ConsortiumD Ford, D F Easton, M Stratton, et al.
Journal of Medical Genetics|June 1, 2005
Genetic, functional, and histopathological evaluation of two C-terminal BRCA1 missense variantsP K Lovelock, S Healey, W Au, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 31, 2000
The pathology of familial breast cancer: histological features of cancers in families not attributable to mutations in BRCA1 or BRCA2S R Lakhani, B A Gusterson, J Jacquemier, et al.
American Journal of Human Genetics|June 19, 1998
Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international studyS L Neuhausen, A K Godwin, R Gershoni-Baruch, et al.
American Journal of Human Genetics|July 31, 1998
Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disordersS Giraud, C X Zhang, O Serova-Sinilnikova, et al.
Journal of the National Cancer Institute|August 13, 1998
Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutationsS R Lakhani, J Jacquemier, J P Sloane, et al.
British Journal of Cancer|November 19, 2009
Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA)A Osorio, R L Milne, G Pita, et al.
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