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Madhuri R Hegde

Showing results (1-10 of 45) with videos related to

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The Journal of Pediatrics|November 15, 2012
Marching towards personalized genomic medicineMadhuri R Hegde
Clinics in Perinatology|June 5, 2015
Gamut of genetic testing for neonatal careArunkanth Ankala, Madhuri R Hegde
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
Human Mutation|December 13, 2016
Gene Variant Databases and Sharing: Creating a Global Genomic Variant Database for Personalized MedicineLora J H Bean, Madhuri R Hegde
Genome Medicine|December 20, 2017
Clinical implications and considerations for evaluation of in silico algorithms for use with ACMG/AMP clinical variant interpretation guidelinesLora J H Bean, Madhuri R Hegde
Human Mutation|March 3, 2016
Gene Variant Databases and Sharing: Creating a Global Genomic Variant Database for Personalized MedicineLora J H Bean, Madhuri R Hegde
Molecular Genetics and Metabolism Reports|April 24, 2026
Identification of Multiple Sulfatase Deficiency (MSD) in newborn screening: A case studyTaraka R Donti, James C DiPerna, Madhuri R Hegde, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2015
Response to SaulYuan Xue, Arunkanth Ankala, William R Wilcox, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 19, 2014
Solving the molecular diagnostic testing conundrum for Mendelian disorders in the era of next-generation sequencing: single-gene, gene panel, or exome/genome sequencingYuan Xue, Arunkanth Ankala, William R Wilcox, et al.
Pageof 5

Showing results (1-10 of 45) with videos related to

Sort By:
Pageof 5
The Journal of Pediatrics|November 15, 2012
Marching towards personalized genomic medicineMadhuri R Hegde
Clinics in Perinatology|June 5, 2015
Gamut of genetic testing for neonatal careArunkanth Ankala, Madhuri R Hegde
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
Human Mutation|December 13, 2016
Gene Variant Databases and Sharing: Creating a Global Genomic Variant Database for Personalized MedicineLora J H Bean, Madhuri R Hegde
Genome Medicine|December 20, 2017
Clinical implications and considerations for evaluation of in silico algorithms for use with ACMG/AMP clinical variant interpretation guidelinesLora J H Bean, Madhuri R Hegde
Human Mutation|March 3, 2016
Gene Variant Databases and Sharing: Creating a Global Genomic Variant Database for Personalized MedicineLora J H Bean, Madhuri R Hegde
Molecular Genetics and Metabolism Reports|April 24, 2026
Identification of Multiple Sulfatase Deficiency (MSD) in newborn screening: A case studyTaraka R Donti, James C DiPerna, Madhuri R Hegde, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2015
Response to SaulYuan Xue, Arunkanth Ankala, William R Wilcox, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 19, 2014
Solving the molecular diagnostic testing conundrum for Mendelian disorders in the era of next-generation sequencing: single-gene, gene panel, or exome/genome sequencingYuan Xue, Arunkanth Ankala, William R Wilcox, et al.
Pageof 5