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Cancer Research
|
March 21, 1998
Consortium study on 1280 breast carcinomas: allelic loss on chromosome 17 targets subregions associated with family history and clinical parameters
C M Phelan, A Borg, M Cuny, 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 study
S L Neuhausen, A K Godwin, R Gershoni-Baruch, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
February 15, 2003
The Italian multi-centre project on evaluation of MRI and other imaging modalities in early detection of breast cancer in subjects at high genetic risk
F Podo, F Sardanelli, R Canese, et al.
British Journal of Cancer
|
March 24, 2011
Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2
A Osorio, R L Milne, R Alonso, 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.
Page
of 5
Search research articles
Search
Showing results (41-50 of 45) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 45 results.
Cancer Research
|
March 21, 1998
Consortium study on 1280 breast carcinomas: allelic loss on chromosome 17 targets subregions associated with family history and clinical parameters
C M Phelan, A Borg, M Cuny, 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 study
S L Neuhausen, A K Godwin, R Gershoni-Baruch, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
February 15, 2003
The Italian multi-centre project on evaluation of MRI and other imaging modalities in early detection of breast cancer in subjects at high genetic risk
F Podo, F Sardanelli, R Canese, et al.
British Journal of Cancer
|
March 24, 2011
Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2
A Osorio, R L Milne, R Alonso, 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.
Page
of 5