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American Journal of Medical Genetics. Part A
|
September 9, 2016
Somatic-gonadal mosaicism causing Sotos syndrome
Benjamin Kamien, Tessa Dadd, Melissa Buckman, et al.
International Journal of Cancer
|
November 22, 2007
Aurora-A and Cyclin D1 polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer
Bente A Talseth, Katie A Ashton, Cliff Meldrum, et al.
Cancer Epidemiology
|
October 7, 2011
DNA repair gene polymorphisms and risk of early onset colorectal cancer in Lynch syndrome
Stuart G Reeves, Cliff Meldrum, Claire Groombridge, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association
|
August 11, 2007
The PAI-1 4G/5G gene polymorphism and ischemic stroke: an association study and meta-analysis
John Attia, Ammarin Thakkinstian, Yang Wang, et al.
Journal of Cancer Research and Clinical Oncology
|
August 30, 2002
Impact of microsatellite testing and mismatch repair protein expression on the clinical interpretation of genetic testing in hereditary non-polyposis colorectal cancer
Robyn Ward, Cliff Meldrum, Rachael Williams, et al.
ANZ Journal of Surgery
|
November 23, 2012
Clinicopathological and molecular aspects of foregut gastrointestinal stromal tumours
Jason Chen, Justin S Gundara, Richard Haddad, et al.
European Journal of Medical Genetics
|
October 18, 2015
Narrowing the critical region for overgrowth within 13q14.2-q14.3 microdeletions
Benjamin Kamien, M Cristina Digilio, Antonio Novelli, et al.
European Journal of Human Genetics : EJHG
|
January 22, 2009
MTHFR 677 C>T and 1298 A>C polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer
Stuart G Reeves, Cliff Meldrum, Claire Groombridge, et al.
BMC Medical Genomics
|
March 28, 2013
Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients
Bente A Talseth-Palmer, Elizabeth G Holliday, Tiffany-Jane Evans, et al.
Human Mutation
|
February 10, 2015
AmpliVar: mutation detection in high-throughput sequence from amplicon-based libraries
Arthur L Hsu, Olga Kondrashova, Sebastian Lunke, et al.
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of 3
Search research articles
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Showing results (11-20 of 28) with videos related to
Sort By:
Page
of 3
American Journal of Medical Genetics. Part A
|
September 9, 2016
Somatic-gonadal mosaicism causing Sotos syndrome
Benjamin Kamien, Tessa Dadd, Melissa Buckman, et al.
International Journal of Cancer
|
November 22, 2007
Aurora-A and Cyclin D1 polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer
Bente A Talseth, Katie A Ashton, Cliff Meldrum, et al.
Cancer Epidemiology
|
October 7, 2011
DNA repair gene polymorphisms and risk of early onset colorectal cancer in Lynch syndrome
Stuart G Reeves, Cliff Meldrum, Claire Groombridge, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association
|
August 11, 2007
The PAI-1 4G/5G gene polymorphism and ischemic stroke: an association study and meta-analysis
John Attia, Ammarin Thakkinstian, Yang Wang, et al.
Journal of Cancer Research and Clinical Oncology
|
August 30, 2002
Impact of microsatellite testing and mismatch repair protein expression on the clinical interpretation of genetic testing in hereditary non-polyposis colorectal cancer
Robyn Ward, Cliff Meldrum, Rachael Williams, et al.
ANZ Journal of Surgery
|
November 23, 2012
Clinicopathological and molecular aspects of foregut gastrointestinal stromal tumours
Jason Chen, Justin S Gundara, Richard Haddad, et al.
European Journal of Medical Genetics
|
October 18, 2015
Narrowing the critical region for overgrowth within 13q14.2-q14.3 microdeletions
Benjamin Kamien, M Cristina Digilio, Antonio Novelli, et al.
European Journal of Human Genetics : EJHG
|
January 22, 2009
MTHFR 677 C>T and 1298 A>C polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer
Stuart G Reeves, Cliff Meldrum, Claire Groombridge, et al.
BMC Medical Genomics
|
March 28, 2013
Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients
Bente A Talseth-Palmer, Elizabeth G Holliday, Tiffany-Jane Evans, et al.
Human Mutation
|
February 10, 2015
AmpliVar: mutation detection in high-throughput sequence from amplicon-based libraries
Arthur L Hsu, Olga Kondrashova, Sebastian Lunke, et al.
Page
of 3