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A D Roses

Showing results (251-260 of 347) with videos related to

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American Journal of Human Genetics|June 1, 1992
Recombination of 4p16 DNA markers in an unusual family with Huntington diseaseC Pritchard, N Zhu, J Zuo, et al.
Genomics|July 20, 1995
Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4AK B Othmane, D Loeb, R Hayworth-Hodgte, et al.
Human Molecular Genetics|October 1, 1993
Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8qK Ben Othmane, F Hentati, F Lennon, et al.
Genomics|March 1, 1990
Confirmation of linkage in von Hippel-Lindau diseaseJ M Vance, K W Small, M A Jones, et al.
Progress in Clinical and Biological Research|January 1, 1989
Linkage studies in familial Alzheimer's diseaseA D Roses, M A Pericak-Vance, L Yamaoka, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Linkage studies in tuberous sclerosis. Chromosome 9?, 11?, or maybe 14!R S Kandt, M A Pericak-Vance, W Y Hung, et al.
Annals of Neurology|May 1, 1997
Endoglin gene polymorphism as a risk factor for sporadic intracerebral hemorrhageM J Alberts, J P Davis, C Graffagnino, et al.
The Pharmacogenomics Journal|August 11, 2004
Identification of a pharmacogenetic effect by linkage disequilibrium mappingC-F Xu, K F Lewis, A J Yeo, et al.
Journal of Medical Genetics|September 1, 1987
Linkage analysis of peripheral neurofibromatosis to DNA markers on chromosome 8S R Diehl, M Boehnke, F S Collins, et al.
Arzneimittel-Forschung|March 1, 1995
Influence of the susceptibility genes apolipoprotein E-epsilon 4 and apolipoprotein E-epsilon 2 on the rate of disease expressivity of late-onset Alzheimer's diseaseA D Roses, A M Saunders, E H Corder, et al.
Pageof 35

Showing results (251-260 of 347) with videos related to

Sort By:
Pageof 35
American Journal of Human Genetics|June 1, 1992
Recombination of 4p16 DNA markers in an unusual family with Huntington diseaseC Pritchard, N Zhu, J Zuo, et al.
Genomics|July 20, 1995
Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4AK B Othmane, D Loeb, R Hayworth-Hodgte, et al.
Human Molecular Genetics|October 1, 1993
Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8qK Ben Othmane, F Hentati, F Lennon, et al.
Genomics|March 1, 1990
Confirmation of linkage in von Hippel-Lindau diseaseJ M Vance, K W Small, M A Jones, et al.
Progress in Clinical and Biological Research|January 1, 1989
Linkage studies in familial Alzheimer's diseaseA D Roses, M A Pericak-Vance, L Yamaoka, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Linkage studies in tuberous sclerosis. Chromosome 9?, 11?, or maybe 14!R S Kandt, M A Pericak-Vance, W Y Hung, et al.
Annals of Neurology|May 1, 1997
Endoglin gene polymorphism as a risk factor for sporadic intracerebral hemorrhageM J Alberts, J P Davis, C Graffagnino, et al.
The Pharmacogenomics Journal|August 11, 2004
Identification of a pharmacogenetic effect by linkage disequilibrium mappingC-F Xu, K F Lewis, A J Yeo, et al.
Journal of Medical Genetics|September 1, 1987
Linkage analysis of peripheral neurofibromatosis to DNA markers on chromosome 8S R Diehl, M Boehnke, F S Collins, et al.
Arzneimittel-Forschung|March 1, 1995
Influence of the susceptibility genes apolipoprotein E-epsilon 4 and apolipoprotein E-epsilon 2 on the rate of disease expressivity of late-onset Alzheimer's diseaseA D Roses, A M Saunders, E H Corder, et al.
Pageof 35