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J M Vance

Showing results (21-30 of 104) with videos related to

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Annals of Human Genetics|January 22, 2008
Gene-gene interaction between FGF20 and MAOB in Parkinson diseaseX Gao, W K Scott, G Wang, et al.
Cytogenetics and Cell Genetics|January 1, 1978
Genetic linkage studies in Huntington diseaseM A Pericak-Vance, P M Conneally, A D Merritt, et al.
Human Mutation|May 2, 2000
Identification of seven novel SNPS (five nucleotide and two amino acid substitutions) in the connexin31 (GJB3) geneN López-Bigas, R Rabionet, E Martínez, et al.
Clinical Genetics|August 1, 1981
Carrier detection in Sanfilippo syndrome type B: report of six familiesJ M Vance, P M Conneally, R S Wappner, et al.
Journal of Medical Genetics|June 3, 2004
Haplotype analysis of human AMPD1 gene: origin of common mutant alleleK Toyama, H Morisaki, Y Kitamura, et al.
Cytogenetics and Cell Genetics|March 7, 2000
Report of the fifth international workshop on human chromosome 1 mapping 1999P S White, A Forus, T C Matise, et al.
Human Heredity|November 14, 1998
Evidence for genetic heterogeneity supports clinical differences in congenital myasthenic syndromesM M Menold, M Sadeh, F Lennon, et al.
American Journal of Human Genetics|April 1, 1996
Linkage of a gene for macular corneal dystrophy to chromosome 16J M Vance, F Jonasson, F Lennon, et al.
Science (New York, N.Y.)|July 18, 1997
Genetic complexity and Parkinson's disease. Deane Laboratory Parkinson Disease Research GroupW K Scott, J M Staijich, L H Yamaoka, et al.
Genomics|January 25, 2000
Autistic disorder and chromosome 15q11-q13: construction and analysis of a BAC/PAC contigL O Maddox, M M Menold, M P Bass, et al.
Pageof 11

Showing results (21-30 of 104) with videos related to

Sort By:
Pageof 11
Annals of Human Genetics|January 22, 2008
Gene-gene interaction between FGF20 and MAOB in Parkinson diseaseX Gao, W K Scott, G Wang, et al.
Cytogenetics and Cell Genetics|January 1, 1978
Genetic linkage studies in Huntington diseaseM A Pericak-Vance, P M Conneally, A D Merritt, et al.
Human Mutation|May 2, 2000
Identification of seven novel SNPS (five nucleotide and two amino acid substitutions) in the connexin31 (GJB3) geneN López-Bigas, R Rabionet, E Martínez, et al.
Clinical Genetics|August 1, 1981
Carrier detection in Sanfilippo syndrome type B: report of six familiesJ M Vance, P M Conneally, R S Wappner, et al.
Journal of Medical Genetics|June 3, 2004
Haplotype analysis of human AMPD1 gene: origin of common mutant alleleK Toyama, H Morisaki, Y Kitamura, et al.
Cytogenetics and Cell Genetics|March 7, 2000
Report of the fifth international workshop on human chromosome 1 mapping 1999P S White, A Forus, T C Matise, et al.
Human Heredity|November 14, 1998
Evidence for genetic heterogeneity supports clinical differences in congenital myasthenic syndromesM M Menold, M Sadeh, F Lennon, et al.
American Journal of Human Genetics|April 1, 1996
Linkage of a gene for macular corneal dystrophy to chromosome 16J M Vance, F Jonasson, F Lennon, et al.
Science (New York, N.Y.)|July 18, 1997
Genetic complexity and Parkinson's disease. Deane Laboratory Parkinson Disease Research GroupW K Scott, J M Staijich, L H Yamaoka, et al.
Genomics|January 25, 2000
Autistic disorder and chromosome 15q11-q13: construction and analysis of a BAC/PAC contigL O Maddox, M M Menold, M P Bass, et al.
Pageof 11