Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M R Hegde

Showing results (1-10 of 7) with videos related to

Pageof 1
Sort By:
Human Genetics|August 1, 2009
Novel human pathological mutations. Gene symbol: HEXA. Disease: Tay-Sachs diseaseEphrem Chin, L Bean, B Coffee, et al.
Molecular and Cellular Probes|August 11, 1999
Comparative semi-automated analysis of (CAG) repeats in the Huntington disease gene: use of internal standardsL C Williams, M R Hegde, G Herrera, et al.
Genetic Testing|September 12, 2001
Compound heterozygosity at the FMR1 geneM R Hegde, M Fawkner, B Chong, et al.
The Indian Journal of Medical Research|March 30, 2002
Clinical & genetic analysis of four patients with distal upper limb spinal muscular atrophyM R Hegde, B Chong, C Stevenson, et al.
Genetic Testing|May 4, 2000
Null alleles at the Huntington disease locus: implications for diagnostics and CAG repeat instabilityL C Williams, M R Hegde, R Nagappan, et al.
Human Mutation|November 3, 2000
Hierarchical mutation screening protocol for the BRCA1 geneM R Hegde, B Chong, M J Fawkner, et al.
Journal of Medical Genetics|September 22, 2001
Microdeletion in the FMR-1 gene: an apparent null allele using routine clinical PCR amplificationM R Hegde, B Chong, M Fawkner, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Human Genetics|August 1, 2009
Novel human pathological mutations. Gene symbol: HEXA. Disease: Tay-Sachs diseaseEphrem Chin, L Bean, B Coffee, et al.
Molecular and Cellular Probes|August 11, 1999
Comparative semi-automated analysis of (CAG) repeats in the Huntington disease gene: use of internal standardsL C Williams, M R Hegde, G Herrera, et al.
Genetic Testing|September 12, 2001
Compound heterozygosity at the FMR1 geneM R Hegde, M Fawkner, B Chong, et al.
The Indian Journal of Medical Research|March 30, 2002
Clinical & genetic analysis of four patients with distal upper limb spinal muscular atrophyM R Hegde, B Chong, C Stevenson, et al.
Genetic Testing|May 4, 2000
Null alleles at the Huntington disease locus: implications for diagnostics and CAG repeat instabilityL C Williams, M R Hegde, R Nagappan, et al.
Human Mutation|November 3, 2000
Hierarchical mutation screening protocol for the BRCA1 geneM R Hegde, B Chong, M J Fawkner, et al.
Journal of Medical Genetics|September 22, 2001
Microdeletion in the FMR-1 gene: an apparent null allele using routine clinical PCR amplificationM R Hegde, B Chong, M Fawkner, et al.
Pageof 1