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Journal of Medical Genetics
|
September 1, 1987
Linkage studies in peripheral neurofibromatosis
M A Pericak-Vance, L H Yamaoka, J M Vance, et al.
Neurogenetics
|
December 14, 1999
No association between the HLA-A2 allele and Alzheimer disease
G W Small, W K Scott, S Komo, et al.
Clinical Pharmacology and Therapeutics
|
December 20, 2012
Using genetics to enable studies on the prevention of Alzheimer's disease
D G Crenshaw, W K Gottschalk, M W Lutz, et al.
Neuroreport
|
May 27, 1997
Relation of age and apolipoprotein E to cognitive function in Down syndrome adults
G E Alexander, A M Saunders, J Szczepanik, 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 heterogeneity
K Ben Othmane, L T Middleton, L J Loprest, 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 mutation
J 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 disease
W K Scott, A M Saunders, P C Gaskell, et al.
American Journal of Human Genetics
|
March 11, 2000
Fine mapping of the chromosome 12 late-onset Alzheimer disease locus: potential genetic and phenotypic heterogeneity
W K Scott, J M Grubber, P M Conneally, et al.
Advances in Neurology
|
January 1, 1990
Linkage studies of late-onset familial Alzheimer's disease
A D Roses, M A Pericak-Vance, C M Clark, et al.
American Journal of Human Genetics
|
December 1, 1996
Linkage of frontotemporal dementia to chromosome 17: clinical and neuropathological characterization of phenotype
L H Yamaoka, K A Welsh-Bohmer, C M Hulette, et al.
Page
of 35
Search research articles
Search
Showing results (301-310 of 347) with videos related to
Sort By:
Page
of 35
Journal of Medical Genetics
|
September 1, 1987
Linkage studies in peripheral neurofibromatosis
M A Pericak-Vance, L H Yamaoka, J M Vance, et al.
Neurogenetics
|
December 14, 1999
No association between the HLA-A2 allele and Alzheimer disease
G W Small, W K Scott, S Komo, et al.
Clinical Pharmacology and Therapeutics
|
December 20, 2012
Using genetics to enable studies on the prevention of Alzheimer's disease
D G Crenshaw, W K Gottschalk, M W Lutz, et al.
Neuroreport
|
May 27, 1997
Relation of age and apolipoprotein E to cognitive function in Down syndrome adults
G E Alexander, A M Saunders, J Szczepanik, 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 heterogeneity
K Ben Othmane, L T Middleton, L J Loprest, 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 mutation
J 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 disease
W K Scott, A M Saunders, P C Gaskell, et al.
American Journal of Human Genetics
|
March 11, 2000
Fine mapping of the chromosome 12 late-onset Alzheimer disease locus: potential genetic and phenotypic heterogeneity
W K Scott, J M Grubber, P M Conneally, et al.
Advances in Neurology
|
January 1, 1990
Linkage studies of late-onset familial Alzheimer's disease
A D Roses, M A Pericak-Vance, C M Clark, et al.
American Journal of Human Genetics
|
December 1, 1996
Linkage of frontotemporal dementia to chromosome 17: clinical and neuropathological characterization of phenotype
L H Yamaoka, K A Welsh-Bohmer, C M Hulette, et al.
Page
of 35