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Oncogene
|
September 1, 1991
Detection of transforming genes by transfection of DNA from primary soft-tissue tumours
S Gill, M R Stratton, H Patterson, et al.
The Journal of Pathology
|
January 12, 2000
Genetic alterations in 'normal' luminal and myoepithelial cells of the breast
S R Lakhani, R Chaggar, S Davies, et al.
Nature Genetics
|
January 1, 1997
Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene
S A Gayther, J Mangion, P Russell, et al.
Journal of Medical Genetics
|
March 21, 1998
Using gene carrier probability to select high risk families for identifying germline mutations in breast cancer susceptibility genes
J Chang-Claude, J Dong, S Schmidt, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
December 6, 2000
BRCA1 and BRCA2 mutations in breast cancer families with multiple primary cancers
H A Shih, K L Nathanson, S Seal, et al.
British Journal of Cancer
|
November 1, 1995
Loss of heterozygosity in sporadic breast tumours at the BRCA2 locus on chromosome 13q12-q13
A M Cleton-Jansen, N Collins, S R Lakhani, et al.
American Journal of Medical Genetics
|
December 26, 2001
Case of interstitial 12q deletion in association with Wilms tumor
E A Rapley, D Hargrave, N Persinguhe, et al.
Nature Genetics
|
December 1, 1995
Familial cylindromatosis (turban tumour syndrome) gene localised to chromosome 16q12-q13: evidence for its role as a tumour suppressor gene
P J Biggs, R Wooster, D Ford, et al.
Nature Genetics
|
August 1, 1996
Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-q21
N Rahman, L Arbour, P Tonin, et al.
Journal of the National Cancer Institute
|
June 8, 1999
Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer
J Peto, N Collins, R Barfoot, et al.
Page
of 10
Search research articles
Search
Showing results (41-50 of 97) with videos related to
Sort By:
Page
of 10
Oncogene
|
September 1, 1991
Detection of transforming genes by transfection of DNA from primary soft-tissue tumours
S Gill, M R Stratton, H Patterson, et al.
The Journal of Pathology
|
January 12, 2000
Genetic alterations in 'normal' luminal and myoepithelial cells of the breast
S R Lakhani, R Chaggar, S Davies, et al.
Nature Genetics
|
January 1, 1997
Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene
S A Gayther, J Mangion, P Russell, et al.
Journal of Medical Genetics
|
March 21, 1998
Using gene carrier probability to select high risk families for identifying germline mutations in breast cancer susceptibility genes
J Chang-Claude, J Dong, S Schmidt, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
December 6, 2000
BRCA1 and BRCA2 mutations in breast cancer families with multiple primary cancers
H A Shih, K L Nathanson, S Seal, et al.
British Journal of Cancer
|
November 1, 1995
Loss of heterozygosity in sporadic breast tumours at the BRCA2 locus on chromosome 13q12-q13
A M Cleton-Jansen, N Collins, S R Lakhani, et al.
American Journal of Medical Genetics
|
December 26, 2001
Case of interstitial 12q deletion in association with Wilms tumor
E A Rapley, D Hargrave, N Persinguhe, et al.
Nature Genetics
|
December 1, 1995
Familial cylindromatosis (turban tumour syndrome) gene localised to chromosome 16q12-q13: evidence for its role as a tumour suppressor gene
P J Biggs, R Wooster, D Ford, et al.
Nature Genetics
|
August 1, 1996
Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-q21
N Rahman, L Arbour, P Tonin, et al.
Journal of the National Cancer Institute
|
June 8, 1999
Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer
J Peto, N Collins, R Barfoot, et al.
Page
of 10