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Proceedings of the National Academy of Sciences of the United States of America
|
March 15, 2001
A single nucleotide polymorphism in the RAD51 gene modifies cancer risk in BRCA2 but not BRCA1 carriers
E Levy-Lahad, A Lahad, S Eisenberg, et al.
British Journal of Cancer
|
July 30, 2014
Overall survival and clinical characteristics of pancreatic cancer in BRCA mutation carriers
T Golan, Z S Kanji, R Epelbaum, et al.
American Journal of Human Genetics
|
October 3, 1998
Double heterozygotes for the Ashkenazi founder mutations in BRCA1 and BRCA2 genes
E Friedman, R Bar-Sade Bruchim, A Kruglikova, et al.
Human Mutation
|
January 11, 2000
Mutational analyses of BRCA1 and BRCA2 in Ashkenazi and non-Ashkenazi Jewish women with familial breast and ovarian cancer
R Shiri-Sverdlov, P Oefner, L Green, et al.
Neurology
|
February 11, 2012
The LRRK2 G2019S mutation is associated with Parkinson disease and concomitant non-skin cancers
R Inzelberg, O S Cohen, J Aharon-Peretz, 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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of 3
Search research articles
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Showing results (21-30 of 26) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 26 results.
Proceedings of the National Academy of Sciences of the United States of America
|
March 15, 2001
A single nucleotide polymorphism in the RAD51 gene modifies cancer risk in BRCA2 but not BRCA1 carriers
E Levy-Lahad, A Lahad, S Eisenberg, et al.
British Journal of Cancer
|
July 30, 2014
Overall survival and clinical characteristics of pancreatic cancer in BRCA mutation carriers
T Golan, Z S Kanji, R Epelbaum, et al.
American Journal of Human Genetics
|
October 3, 1998
Double heterozygotes for the Ashkenazi founder mutations in BRCA1 and BRCA2 genes
E Friedman, R Bar-Sade Bruchim, A Kruglikova, et al.
Human Mutation
|
January 11, 2000
Mutational analyses of BRCA1 and BRCA2 in Ashkenazi and non-Ashkenazi Jewish women with familial breast and ovarian cancer
R Shiri-Sverdlov, P Oefner, L Green, et al.
Neurology
|
February 11, 2012
The LRRK2 G2019S mutation is associated with Parkinson disease and concomitant non-skin cancers
R Inzelberg, O S Cohen, J Aharon-Peretz, 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 3