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The New England Journal of Medicine
|
February 16, 2007
Inheritance of a cancer-associated MLH1 germ-line epimutation
Megan P Hitchins, Justin J L Wong, Graeme Suthers, et al.
American Journal of Medical Genetics. Part A
|
September 20, 2012
Disease-specific databases: why we need them and some recommendations from the Human Variome Project Meeting, May 28, 2011
Heather J Howard, Arthur Beaudet, Vera Gil-da-Silva Lopes, et al.
Breast Cancer Research : BCR
|
June 26, 2004
Frequency of the ATM IVS10-6T-->G variant in Australian multiple-case breast cancer families
Geoffrey J Lindeman, Melody Hiew, Jane E Visvader, et al.
Genes, Chromosomes & Cancer
|
September 27, 2006
Characterization of the breast cancer associated ATM 7271T>G (V2424G) mutation by gene expression profiling
Nic Waddell, Jyoti Jonnalagadda, Anna Marsh, et al.
Gastroenterology
|
November 16, 2005
MLH1 germline epimutations as a factor in hereditary nonpolyposis colorectal cancer
Megan Hitchins, Rachel Williams, Kayfong Cheong, et al.
Mutation Research
|
November 11, 2008
Analysis of a set of missense, frameshift, and in-frame deletion variants of BRCA1
Marcelo Carvalho, Maria A Pino, Rachel Karchin, et al.
Breast Cancer Research : BCR
|
March 2, 2006
Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resource
Graham J Mann, Heather Thorne, Rosemary L Balleine, et al.
Atherosclerosis. Supplements
|
September 16, 2011
Familial hypercholesterolaemia: a model of care for Australasia
Gerald F Watts, David R Sullivan, Nicola Poplawski, et al.
Journal of the National Cancer Institute
|
December 24, 2009
Risks of Lynch syndrome cancers for MSH6 mutation carriers
Laura Baglietto, Noralane M Lindor, James G Dowty, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 29) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 29 results.
The New England Journal of Medicine
|
February 16, 2007
Inheritance of a cancer-associated MLH1 germ-line epimutation
Megan P Hitchins, Justin J L Wong, Graeme Suthers, et al.
American Journal of Medical Genetics. Part A
|
September 20, 2012
Disease-specific databases: why we need them and some recommendations from the Human Variome Project Meeting, May 28, 2011
Heather J Howard, Arthur Beaudet, Vera Gil-da-Silva Lopes, et al.
Breast Cancer Research : BCR
|
June 26, 2004
Frequency of the ATM IVS10-6T-->G variant in Australian multiple-case breast cancer families
Geoffrey J Lindeman, Melody Hiew, Jane E Visvader, et al.
Genes, Chromosomes & Cancer
|
September 27, 2006
Characterization of the breast cancer associated ATM 7271T>G (V2424G) mutation by gene expression profiling
Nic Waddell, Jyoti Jonnalagadda, Anna Marsh, et al.
Gastroenterology
|
November 16, 2005
MLH1 germline epimutations as a factor in hereditary nonpolyposis colorectal cancer
Megan Hitchins, Rachel Williams, Kayfong Cheong, et al.
Mutation Research
|
November 11, 2008
Analysis of a set of missense, frameshift, and in-frame deletion variants of BRCA1
Marcelo Carvalho, Maria A Pino, Rachel Karchin, et al.
Breast Cancer Research : BCR
|
March 2, 2006
Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resource
Graham J Mann, Heather Thorne, Rosemary L Balleine, et al.
Atherosclerosis. Supplements
|
September 16, 2011
Familial hypercholesterolaemia: a model of care for Australasia
Gerald F Watts, David R Sullivan, Nicola Poplawski, et al.
Journal of the National Cancer Institute
|
December 24, 2009
Risks of Lynch syndrome cancers for MSH6 mutation carriers
Laura Baglietto, Noralane M Lindor, James G Dowty, et al.
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of 3