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A D Roses

Showing results (291-300 of 347) with videos related to

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Nucleic Acids Research|September 26, 1988
A Bgl II polymorphism detected by LDR152 [D19S19]A P Walker, R J Bartlett, L H Yamaoka, et al.
Annals of Neurology|November 1, 1996
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13J M Stajich, J M Gilchrist, F Lennon, et al.
Nucleic Acids Research|February 25, 1991
MspI RFLP for microtubule associated protein-2 (MAP2)M J Alberts, R S Kandt, M A Pericak-Vance, et al.
The Annals of Thoracic Surgery|October 6, 1997
Preliminary report of a genetic basis for cognitive decline after cardiac operations. The Neurologic Outcome Research Group of the Duke Heart CenterB E Tardiff, M F Newman, A M Saunders, et al.
Progress in Clinical and Biological Research|January 1, 1989
Sib-pair linkage analysis in late onset Alzheimer's diseaseD V Dawson, A D Roses, M A Pericak-Vance, et al.
Genetic Epidemiology|January 1, 1993
Linkage analysis in familial Alzheimer disease: description of the Duke and Boston data setsM A Pericak-Vance, P H St George-Hyslop, P C Gaskell, et al.
The Pharmacogenomics Journal|December 3, 2003
A Gilbert's syndrome UGT1A1 variant confers susceptibility to tranilast-induced hyperbilirubinemiaT M Danoff, D A Campbell, L C McCarthy, et al.
Australian Paediatric Journal|January 1, 1988
Myotonic dystrophy: update on progress to define the geneA D Roses, M A Pericak-Vance, R J Bartlett, 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.
Genomics|May 1, 1992
An error in dystrophin mRNA processing in golden retriever muscular dystrophy, an animal homologue of Duchenne muscular dystrophyN J Sharp, J N Kornegay, S D Van Camp, et al.
Pageof 35

Showing results (291-300 of 347) with videos related to

Sort By:
Pageof 35
Nucleic Acids Research|September 26, 1988
A Bgl II polymorphism detected by LDR152 [D19S19]A P Walker, R J Bartlett, L H Yamaoka, et al.
Annals of Neurology|November 1, 1996
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13J M Stajich, J M Gilchrist, F Lennon, et al.
Nucleic Acids Research|February 25, 1991
MspI RFLP for microtubule associated protein-2 (MAP2)M J Alberts, R S Kandt, M A Pericak-Vance, et al.
The Annals of Thoracic Surgery|October 6, 1997
Preliminary report of a genetic basis for cognitive decline after cardiac operations. The Neurologic Outcome Research Group of the Duke Heart CenterB E Tardiff, M F Newman, A M Saunders, et al.
Progress in Clinical and Biological Research|January 1, 1989
Sib-pair linkage analysis in late onset Alzheimer's diseaseD V Dawson, A D Roses, M A Pericak-Vance, et al.
Genetic Epidemiology|January 1, 1993
Linkage analysis in familial Alzheimer disease: description of the Duke and Boston data setsM A Pericak-Vance, P H St George-Hyslop, P C Gaskell, et al.
The Pharmacogenomics Journal|December 3, 2003
A Gilbert's syndrome UGT1A1 variant confers susceptibility to tranilast-induced hyperbilirubinemiaT M Danoff, D A Campbell, L C McCarthy, et al.
Australian Paediatric Journal|January 1, 1988
Myotonic dystrophy: update on progress to define the geneA D Roses, M A Pericak-Vance, R J Bartlett, 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.
Genomics|May 1, 1992
An error in dystrophin mRNA processing in golden retriever muscular dystrophy, an animal homologue of Duchenne muscular dystrophyN J Sharp, J N Kornegay, S D Van Camp, et al.
Pageof 35