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T Foroud

Showing results (41-50 of 111) with videos related to

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Archives of Neurology|June 1, 1996
Motor changes in presymptomatic Huntington disease gene carriersE Siemers, T Foroud, D J Bill, et al.
Neurology|March 12, 2003
Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson diseaseT Foroud, S K Uniacke, L Liu, et al.
American Journal of Human Genetics|September 16, 1999
Joint multipoint linkage analysis of multivariate qualitative and quantitative traits. II. Alcoholism and event-related potentialsJ T Williams, H Begleiter, B Porjesz, et al.
Nature Genetics|April 1, 1992
Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein geneS R Dlouhy, K Hsiao, M R Farlow, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 24, 2003
Linkage of structure at the proximal femur to chromosomes 3, 7, 8, and 19D L Koller, K E White, G Liu, et al.
Neurology|July 29, 2009
Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutationsN Pankratz, D K Kissell, M W Pauciulo, et al.
Neurology|September 7, 2007
LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8W C Nichols, V E Elsaesser, N Pankratz, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locusI Takacs, D L Koller, M Peacock, et al.
Molecular Psychiatry|December 31, 2003
A genome-wide screen for genes influencing conduct disorderD M Dick, T-K Li, H J Edenberg, et al.
Neurology|July 21, 2006
Saccades in presymptomatic and early stages of Huntington diseaseT Blekher, S A Johnson, J Marshall, et al.
Pageof 12

Showing results (41-50 of 111) with videos related to

Sort By:
Pageof 12
Archives of Neurology|June 1, 1996
Motor changes in presymptomatic Huntington disease gene carriersE Siemers, T Foroud, D J Bill, et al.
Neurology|March 12, 2003
Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson diseaseT Foroud, S K Uniacke, L Liu, et al.
American Journal of Human Genetics|September 16, 1999
Joint multipoint linkage analysis of multivariate qualitative and quantitative traits. II. Alcoholism and event-related potentialsJ T Williams, H Begleiter, B Porjesz, et al.
Nature Genetics|April 1, 1992
Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein geneS R Dlouhy, K Hsiao, M R Farlow, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 24, 2003
Linkage of structure at the proximal femur to chromosomes 3, 7, 8, and 19D L Koller, K E White, G Liu, et al.
Neurology|July 29, 2009
Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutationsN Pankratz, D K Kissell, M W Pauciulo, et al.
Neurology|September 7, 2007
LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8W C Nichols, V E Elsaesser, N Pankratz, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locusI Takacs, D L Koller, M Peacock, et al.
Molecular Psychiatry|December 31, 2003
A genome-wide screen for genes influencing conduct disorderD M Dick, T-K Li, H J Edenberg, et al.
Neurology|July 21, 2006
Saccades in presymptomatic and early stages of Huntington diseaseT Blekher, S A Johnson, J Marshall, et al.
Pageof 12