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Benjamin B Roa

Showing results (1-10 of 33) with videos related to

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Current Protocols in Human Genetics|April 23, 2008
Detecting mutations in the APC gene in familial adenomatous polyposis (FAP)Madhuri R Hegde, Benjamin B Roa
Current Protocols in Human Genetics|April 11, 2009
Genetic testing for hereditary nonpolyposis colorectal cancer (HNPCC)Madhuri R Hegde, Benjamin B Roa
Methods in Molecular Biology (Clifton, N.J.)|December 21, 2002
Denaturing high-performance liquid chromatography and sequence analyses for MECP2 mutations in Rett syndromeInge M Buyse, Benjamin B Roa
Expert Review of Molecular Diagnostics|November 1, 2005
Evolution of prenatal genetics: from point mutation testing to chromosomal microarray analysisBenjamin B Roa, Joseph Pulliam, Christine M Eng, et al.
Clinical Colorectal Cancer|August 23, 2011
Body surface area-based dosing of 5-fluoruracil results in extensive interindividual variability in 5-fluorouracil exposure in colorectal cancer patients on FOLFOX regimensJennifer Saam, Gregory C Critchfield, Stephanie A Hamilton, et al.
American Journal of Human Genetics|December 31, 2005
Interruptions in the expanded ATTCT repeat of spinocerebellar ataxia type 10: repeat purity as a disease modifier?Tohru Matsuura, Ping Fang, Christopher E Pearson, et al.
Human Mutation|September 7, 2019
A substantial proportion of apparently heterozygous TP53 pathogenic variants detected with a next-generation sequencing hereditary pan-cancer panel are acquired somaticallyBradford Coffee, Hannah C Cox, Ryan Bernhisel, et al.
Biomarkers in Medicine|March 28, 2015
Analytical validation of a melanoma diagnostic gene signature using formalin-fixed paraffin-embedded melanocytic lesionsM Bryan Warf, Darl D Flake, Doug Adams, et al.
Future Science OA|September 9, 2017
Analytical validation of a 12-gene molecular test for the prediction of distant recurrence in breast cancerM Bryan Warf, Saradha Rajamani, Kristin Krappmann, et al.
American Journal of Medical Genetics. Part A|March 8, 2008
Infrequency of two deletion mutations at the DFNB1 locus in patients and controlsHsiao-Yuan Tang, Monica J Basehore, Gregory L Blakey, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Current Protocols in Human Genetics|April 23, 2008
Detecting mutations in the APC gene in familial adenomatous polyposis (FAP)Madhuri R Hegde, Benjamin B Roa
Current Protocols in Human Genetics|April 11, 2009
Genetic testing for hereditary nonpolyposis colorectal cancer (HNPCC)Madhuri R Hegde, Benjamin B Roa
Methods in Molecular Biology (Clifton, N.J.)|December 21, 2002
Denaturing high-performance liquid chromatography and sequence analyses for MECP2 mutations in Rett syndromeInge M Buyse, Benjamin B Roa
Expert Review of Molecular Diagnostics|November 1, 2005
Evolution of prenatal genetics: from point mutation testing to chromosomal microarray analysisBenjamin B Roa, Joseph Pulliam, Christine M Eng, et al.
Clinical Colorectal Cancer|August 23, 2011
Body surface area-based dosing of 5-fluoruracil results in extensive interindividual variability in 5-fluorouracil exposure in colorectal cancer patients on FOLFOX regimensJennifer Saam, Gregory C Critchfield, Stephanie A Hamilton, et al.
American Journal of Human Genetics|December 31, 2005
Interruptions in the expanded ATTCT repeat of spinocerebellar ataxia type 10: repeat purity as a disease modifier?Tohru Matsuura, Ping Fang, Christopher E Pearson, et al.
Human Mutation|September 7, 2019
A substantial proportion of apparently heterozygous TP53 pathogenic variants detected with a next-generation sequencing hereditary pan-cancer panel are acquired somaticallyBradford Coffee, Hannah C Cox, Ryan Bernhisel, et al.
Biomarkers in Medicine|March 28, 2015
Analytical validation of a melanoma diagnostic gene signature using formalin-fixed paraffin-embedded melanocytic lesionsM Bryan Warf, Darl D Flake, Doug Adams, et al.
Future Science OA|September 9, 2017
Analytical validation of a 12-gene molecular test for the prediction of distant recurrence in breast cancerM Bryan Warf, Saradha Rajamani, Kristin Krappmann, et al.
American Journal of Medical Genetics. Part A|March 8, 2008
Infrequency of two deletion mutations at the DFNB1 locus in patients and controlsHsiao-Yuan Tang, Monica J Basehore, Gregory L Blakey, et al.
Pageof 4