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Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
August 24, 2005
Use of molecular tumor characteristics to prioritize mismatch repair gene testing in early-onset colorectal cancer
Melissa C Southey, Mark A Jenkins, Leeanne Mead, et al.
Journal of Gastroenterology and Hepatology
|
June 9, 2016
Tumor testing to identify lynch syndrome in two Australian colorectal cancer cohorts
Daniel D Buchanan, Mark Clendenning, Christophe Rosty, et al.
American Journal of Obstetrics & Gynecology MFM
|
November 18, 2022
The Implementation of Preeclampsia Screening and Prevention (IMPRESS) Study
J M Johnson, Jennifer D Walsh, Nanette B Okun, et al.
Familial Cancer
|
August 14, 2014
High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry
Christophe Rosty, Michael D Walsh, Noralane M Lindor, et al.
Familial Cancer
|
February 26, 2009
Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysis
Michael D Walsh, Daniel D Buchanan, Rhiannon Walters, et al.
The Journal of Molecular Diagnostics : JMD
|
November 26, 2015
Analytical Validation and Application of a Targeted Next-Generation Sequencing Mutation-Detection Assay for Use in Treatment Assignment in the NCI-MPACT Trial
Chih-Jian Lih, David J Sims, Robin D Harrington, et al.
Plos One
|
July 30, 2015
Robustness of Next Generation Sequencing on Older Formalin-Fixed Paraffin-Embedded Tissue
Danielle Mercatante Carrick, Michele G Mehaffey, Michael C Sachs, et al.
Pathology
|
December 27, 2011
Using tumour pathology to identify people at high genetic risk of breast and colorectal cancers
J L Hopper, M A Jenkins, J G Dowty, et al.
Immunogenetics
|
July 7, 2011
The role of MHC class I allele Mamu-A*07 during SIV(mac)239 infection
Jason S Reed, John Sidney, Shari M Piaskowski, et al.
American Journal of Human Genetics
|
August 5, 2000
Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III
D F Levinson, P Holmans, R E Straub, et al.
Page
of 95
Search research articles
Search
Showing results (901-910 of 947) with videos related to
Sort By:
Page
of 95
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
August 24, 2005
Use of molecular tumor characteristics to prioritize mismatch repair gene testing in early-onset colorectal cancer
Melissa C Southey, Mark A Jenkins, Leeanne Mead, et al.
Journal of Gastroenterology and Hepatology
|
June 9, 2016
Tumor testing to identify lynch syndrome in two Australian colorectal cancer cohorts
Daniel D Buchanan, Mark Clendenning, Christophe Rosty, et al.
American Journal of Obstetrics & Gynecology MFM
|
November 18, 2022
The Implementation of Preeclampsia Screening and Prevention (IMPRESS) Study
J M Johnson, Jennifer D Walsh, Nanette B Okun, et al.
Familial Cancer
|
August 14, 2014
High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry
Christophe Rosty, Michael D Walsh, Noralane M Lindor, et al.
Familial Cancer
|
February 26, 2009
Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysis
Michael D Walsh, Daniel D Buchanan, Rhiannon Walters, et al.
The Journal of Molecular Diagnostics : JMD
|
November 26, 2015
Analytical Validation and Application of a Targeted Next-Generation Sequencing Mutation-Detection Assay for Use in Treatment Assignment in the NCI-MPACT Trial
Chih-Jian Lih, David J Sims, Robin D Harrington, et al.
Plos One
|
July 30, 2015
Robustness of Next Generation Sequencing on Older Formalin-Fixed Paraffin-Embedded Tissue
Danielle Mercatante Carrick, Michele G Mehaffey, Michael C Sachs, et al.
Pathology
|
December 27, 2011
Using tumour pathology to identify people at high genetic risk of breast and colorectal cancers
J L Hopper, M A Jenkins, J G Dowty, et al.
Immunogenetics
|
July 7, 2011
The role of MHC class I allele Mamu-A*07 during SIV(mac)239 infection
Jason S Reed, John Sidney, Shari M Piaskowski, et al.
American Journal of Human Genetics
|
August 5, 2000
Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III
D F Levinson, P Holmans, R E Straub, et al.
Page
of 95