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J M Vance

Showing results (71-80 of 104) with videos related to

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Ophthalmology|August 12, 1999
Analysis of the Stargardt disease gene (ABCR) in age-related macular degenerationM A De La Paz, V K Guy, S Abou-Donia, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13 in American families suggests the existence of a second causal mutationJ M Stajich, J M Gilchrist, F Lennon, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Report and abstracts of the third international workshop on human chromosome 1 mapping 1997J M Vance, T C Matise, R Wooster, et al.
Genomics|June 15, 1999
Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneityM P Winn, P J Conlon, K L Lynn, et al.
American Journal of Human Genetics|February 11, 1999
Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7M C Speer, J M Vance, J M Grubber, et al.
American Journal of Human Genetics|November 1, 1996
Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutationE M McNally, M R Passos-Bueno, C G Bönnemann, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 26, 2008
Longitudinal follow-up of late-onset Alzheimer disease familiesR M Carney, M A Slifer, P I Lin, et al.
Kidney International|April 14, 1999
Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis. International Collaborative Group for the Study of Familial Focal Segmental GlomerulosclerosisM P Winn, P J Conlon, K L Lynn, et al.
American Journal of Medical Genetics|July 18, 2000
Three probands with autistic disorder and isodicentric chromosome 15C M Wolpert, M M Menold, M P Bass, et al.
Human Heredity|August 7, 1998
Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy familiesM C Speer, J M Vance, F Lennon-Graham, et al.
Pageof 11

Showing results (71-80 of 104) with videos related to

Sort By:
Pageof 11
Ophthalmology|August 12, 1999
Analysis of the Stargardt disease gene (ABCR) in age-related macular degenerationM A De La Paz, V K Guy, S Abou-Donia, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13 in American families suggests the existence of a second causal mutationJ M Stajich, J M Gilchrist, F Lennon, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Report and abstracts of the third international workshop on human chromosome 1 mapping 1997J M Vance, T C Matise, R Wooster, et al.
Genomics|June 15, 1999
Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneityM P Winn, P J Conlon, K L Lynn, et al.
American Journal of Human Genetics|February 11, 1999
Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7M C Speer, J M Vance, J M Grubber, et al.
American Journal of Human Genetics|November 1, 1996
Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutationE M McNally, M R Passos-Bueno, C G Bönnemann, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 26, 2008
Longitudinal follow-up of late-onset Alzheimer disease familiesR M Carney, M A Slifer, P I Lin, et al.
Kidney International|April 14, 1999
Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis. International Collaborative Group for the Study of Familial Focal Segmental GlomerulosclerosisM P Winn, P J Conlon, K L Lynn, et al.
American Journal of Medical Genetics|July 18, 2000
Three probands with autistic disorder and isodicentric chromosome 15C M Wolpert, M M Menold, M P Bass, et al.
Human Heredity|August 7, 1998
Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy familiesM C Speer, J M Vance, F Lennon-Graham, et al.
Pageof 11