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M R Stratton

Showing results (71-80 of 97) with videos related to

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Gastroenterology|March 26, 1999
Inherited susceptibility to colorectal adenomas and carcinomas: evidence for a new predisposition gene on 15q14-q22I Tomlinson, N Rahman, I Frayling, et al.
British Journal of Cancer|February 22, 2000
Lobular carcinoma in situ of the breast is not caused by constitutional mutations in the E-cadherin geneN Rahman, J G Stone, G Coleman, et al.
Journal of Medical Genetics|December 2, 2009
Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility geneI Slade, P Stephens, J Douglas, et al.
British Journal of Cancer|October 10, 2002
HPC2/ELAC2 polymorphisms and prostate cancer risk: analysis by age of onset of diseaseJ C Meitz, S M Edwards, D F Easton, et al.
Oncogene|May 26, 2007
Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromesP M Pollock, M G Gartside, L C Dejeza, et al.
American Journal of Human Genetics|July 1, 1997
Cancer risks in two large breast cancer families linked to BRCA2 on chromosome 13q12-13D F Easton, L Steele, P Fields, et al.
Nature Genetics|November 1, 1996
A polymorphic stop codon in BRCA2S Mazoyer, A M Dunning, O Serova, et al.
British Journal of Cancer|May 14, 1998
A missense mutation in the BRCA2 gene in three siblings with ovarian cancerS Roth, P Kristo, A Auranen, et al.
Human Mutation|January 1, 1997
Screening for ESR mutations in breast and ovarian cancer patientsT I Anderson, R Wooster, K Laake, et al.
British Journal of Cancer|July 20, 2000
Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2E A Rapley, R Barfoot, C Bonaïti-Pellié, et al.
Pageof 10

Showing results (71-80 of 97) with videos related to

Sort By:
Pageof 10
Gastroenterology|March 26, 1999
Inherited susceptibility to colorectal adenomas and carcinomas: evidence for a new predisposition gene on 15q14-q22I Tomlinson, N Rahman, I Frayling, et al.
British Journal of Cancer|February 22, 2000
Lobular carcinoma in situ of the breast is not caused by constitutional mutations in the E-cadherin geneN Rahman, J G Stone, G Coleman, et al.
Journal of Medical Genetics|December 2, 2009
Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility geneI Slade, P Stephens, J Douglas, et al.
British Journal of Cancer|October 10, 2002
HPC2/ELAC2 polymorphisms and prostate cancer risk: analysis by age of onset of diseaseJ C Meitz, S M Edwards, D F Easton, et al.
Oncogene|May 26, 2007
Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromesP M Pollock, M G Gartside, L C Dejeza, et al.
American Journal of Human Genetics|July 1, 1997
Cancer risks in two large breast cancer families linked to BRCA2 on chromosome 13q12-13D F Easton, L Steele, P Fields, et al.
Nature Genetics|November 1, 1996
A polymorphic stop codon in BRCA2S Mazoyer, A M Dunning, O Serova, et al.
British Journal of Cancer|May 14, 1998
A missense mutation in the BRCA2 gene in three siblings with ovarian cancerS Roth, P Kristo, A Auranen, et al.
Human Mutation|January 1, 1997
Screening for ESR mutations in breast and ovarian cancer patientsT I Anderson, R Wooster, K Laake, et al.
British Journal of Cancer|July 20, 2000
Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2E A Rapley, R Barfoot, C Bonaïti-Pellié, et al.
Pageof 10