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J M Vance

Showing results (31-40 of 104) with videos related to

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American Journal of Medical Genetics|January 1, 1980
Evidence of genetic variation for alpha-N-acetyl-D-glucosaminidase in black and white populations: a new polymorphismJ M Vance, M A Pericak-Vance, R C Elston, et al.
Neurogenetics|May 18, 1999
Fine localization of the CMT4A locus using a PAC contig and haplotype analysisK Ben Othmane, J M Rochelle, M Ben Hamida, et al.
American Journal of Medical Genetics|October 1, 1987
Chorea-acanthocytosis: a report of three new families and implications for genetic counsellingJ M Vance, M A Pericak-Vance, M H Bowman, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Report and abstracts of the First International Workshop on Human Chromosome 1 Mapping 1994. Bethesda, Maryland, March 25-27, 1994N C Dracopoli, G A Bruns, G M Brodeur, et al.
Genomics|April 7, 1999
A radiation hybrid breakpoint map of the acute myeloid leukemia (AML) and limb-girdle muscular dystrophy 1A (LGMD1A) regions of chromosome 5q31 localizing 122 expressed sequencesS K Horrigan, L Bartoloni, M C Speer, et al.
Muscle & Nerve|June 1, 1983
Recombinant DNA strategies in genetic neurological diseasesA D Roses, M A Pericak-Vance, L H Yamaoka, et al.
The British Journal of Ophthalmology|May 29, 1998
Coexistence of macular corneal dystrophy types I and II in a single sibshipN P Liu, J Baldwin, F Lennon, et al.
Neurogenetics|March 25, 2000
Further exclusion of FSHD1B from the telomeric region of 10qM C Speer, M A Pericak-Vance, J M Stajich, et al.
Nature Genetics|August 1, 1994
The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American familyJ R Burke, M S Wingfield, K E Lewis, et al.
Nature Medicine|March 1, 1996
Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDHJ R Burke, J J Enghild, M E Martin, et al.
Pageof 11

Showing results (31-40 of 104) with videos related to

Sort By:
Pageof 11
American Journal of Medical Genetics|January 1, 1980
Evidence of genetic variation for alpha-N-acetyl-D-glucosaminidase in black and white populations: a new polymorphismJ M Vance, M A Pericak-Vance, R C Elston, et al.
Neurogenetics|May 18, 1999
Fine localization of the CMT4A locus using a PAC contig and haplotype analysisK Ben Othmane, J M Rochelle, M Ben Hamida, et al.
American Journal of Medical Genetics|October 1, 1987
Chorea-acanthocytosis: a report of three new families and implications for genetic counsellingJ M Vance, M A Pericak-Vance, M H Bowman, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Report and abstracts of the First International Workshop on Human Chromosome 1 Mapping 1994. Bethesda, Maryland, March 25-27, 1994N C Dracopoli, G A Bruns, G M Brodeur, et al.
Genomics|April 7, 1999
A radiation hybrid breakpoint map of the acute myeloid leukemia (AML) and limb-girdle muscular dystrophy 1A (LGMD1A) regions of chromosome 5q31 localizing 122 expressed sequencesS K Horrigan, L Bartoloni, M C Speer, et al.
Muscle & Nerve|June 1, 1983
Recombinant DNA strategies in genetic neurological diseasesA D Roses, M A Pericak-Vance, L H Yamaoka, et al.
The British Journal of Ophthalmology|May 29, 1998
Coexistence of macular corneal dystrophy types I and II in a single sibshipN P Liu, J Baldwin, F Lennon, et al.
Neurogenetics|March 25, 2000
Further exclusion of FSHD1B from the telomeric region of 10qM C Speer, M A Pericak-Vance, J M Stajich, et al.
Nature Genetics|August 1, 1994
The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American familyJ R Burke, M S Wingfield, K E Lewis, et al.
Nature Medicine|March 1, 1996
Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDHJ R Burke, J J Enghild, M E Martin, et al.
Pageof 11