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C Gaskell

Showing results (41-50 of 66) with videos related to

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American Journal of Human Genetics|January 1, 1989
Genetic linkage mapping of chromosome 17 markers and neurofibromatosis type IJ M Vance, M A Pericak-Vance, L H Yamaoka, et al.
Genomics|August 1, 1993
Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneityK Ben Othmane, L T Middleton, L J Loprest, et al.
Nature Genetics|June 1, 1994
Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer diseaseE H Corder, A M Saunders, N J Risch, 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.
Annals of Neurology|October 23, 1997
Apolipoprotein E epsilon2 does not increase risk of early-onset sporadic Alzheimer's diseaseW K Scott, A M Saunders, P C Gaskell, et al.
American Journal of Human Genetics|June 1, 1991
Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkageM A Pericak-Vance, J L Bebout, P C Gaskell, et al.
Neuromuscular Disorders : NMD|September 1, 1994
Development of a microsatellite genetic map spanning 5q31-q33 and subsequent placement of the LGMD1A locus between D5S178 and IL9L H Yamaoka, C A Westbrook, M C Speer, et al.
Experimental Neurology|December 1, 1988
Genetic linkage studies in Alzheimer's disease familiesM A Pericak-Vance, L H Yamaoka, C S Haynes, et al.
Advances in Neurology|January 1, 1990
Linkage studies of late-onset familial Alzheimer's diseaseA D Roses, M A Pericak-Vance, C M Clark, et al.
American Journal of Human Genetics|October 2, 2002
A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)Evan Reid, Mark Kloos, Allison Ashley-Koch, et al.
Pageof 7

Showing results (41-50 of 66) with videos related to

Sort By:
Pageof 7
American Journal of Human Genetics|January 1, 1989
Genetic linkage mapping of chromosome 17 markers and neurofibromatosis type IJ M Vance, M A Pericak-Vance, L H Yamaoka, et al.
Genomics|August 1, 1993
Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneityK Ben Othmane, L T Middleton, L J Loprest, et al.
Nature Genetics|June 1, 1994
Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer diseaseE H Corder, A M Saunders, N J Risch, 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.
Annals of Neurology|October 23, 1997
Apolipoprotein E epsilon2 does not increase risk of early-onset sporadic Alzheimer's diseaseW K Scott, A M Saunders, P C Gaskell, et al.
American Journal of Human Genetics|June 1, 1991
Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkageM A Pericak-Vance, J L Bebout, P C Gaskell, et al.
Neuromuscular Disorders : NMD|September 1, 1994
Development of a microsatellite genetic map spanning 5q31-q33 and subsequent placement of the LGMD1A locus between D5S178 and IL9L H Yamaoka, C A Westbrook, M C Speer, et al.
Experimental Neurology|December 1, 1988
Genetic linkage studies in Alzheimer's disease familiesM A Pericak-Vance, L H Yamaoka, C S Haynes, et al.
Advances in Neurology|January 1, 1990
Linkage studies of late-onset familial Alzheimer's diseaseA D Roses, M A Pericak-Vance, C M Clark, et al.
American Journal of Human Genetics|October 2, 2002
A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)Evan Reid, Mark Kloos, Allison Ashley-Koch, et al.
Pageof 7