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Neurology
|
September 1, 1987
Hereditary motor and sensory neuropathy, X-linked: a half century follow-up
M P Rozear, M A Pericak-Vance, K Fischbeck, et al.
Neurology
|
February 1, 1990
Tight linkage of creatine kinase (CKMM) to myotonic dystrophy on chromosome 19
L H Yamaoka, M A Pericak-Vance, M C Speer, et al.
Science (New York, N.Y.)
|
August 13, 1993
Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families
E H Corder, A M Saunders, W J Strittmatter, et al.
JAMA
|
February 1, 1995
The apolipoprotein E E4 allele and sex-specific risk of Alzheimer's disease
E H Corder, A M Saunders, W J Strittmatter, et al.
American Journal of Human Genetics
|
December 1, 1995
Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy
M C Speer, J M Gilchrist, J G Chutkow, et al.
Journal of Neuropathology and Experimental Neurology
|
August 14, 1999
Neuropathological features of frontotemporal dementia and parkinsonism linked to chromosome 17q21-22 (FTDP-17): Duke Family 1684
C M Hulette, M A Pericak-Vance, A D Roses, et al.
Neuroscience Letters
|
August 11, 1998
No association of alpha1-antichymotrypsin flanking region polymorphism and Alzheimer disease risk in early- and late-onset Alzheimer disease patients
M P Bass, L H Yamaoka, W K Scott, et al.
American Journal of Medical Genetics
|
August 14, 1995
Confirmation of locus heterogeneity in the pure form of familial spastic paraplegia
M C Speer, H M Kingston, R M Boustany, et al.
Neuroscience Letters
|
April 22, 2005
An autosomal genomic screen for dementia in an extended Amish family
A E Ashley-Koch, Y Shao, J B Rimmler, et al.
Annals of Neurology
|
November 1, 1996
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13
J M Stajich, J M Gilchrist, F Lennon, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 66) with videos related to
Sort By:
Page
of 7
Neurology
|
September 1, 1987
Hereditary motor and sensory neuropathy, X-linked: a half century follow-up
M P Rozear, M A Pericak-Vance, K Fischbeck, et al.
Neurology
|
February 1, 1990
Tight linkage of creatine kinase (CKMM) to myotonic dystrophy on chromosome 19
L H Yamaoka, M A Pericak-Vance, M C Speer, et al.
Science (New York, N.Y.)
|
August 13, 1993
Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families
E H Corder, A M Saunders, W J Strittmatter, et al.
JAMA
|
February 1, 1995
The apolipoprotein E E4 allele and sex-specific risk of Alzheimer's disease
E H Corder, A M Saunders, W J Strittmatter, et al.
American Journal of Human Genetics
|
December 1, 1995
Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy
M C Speer, J M Gilchrist, J G Chutkow, et al.
Journal of Neuropathology and Experimental Neurology
|
August 14, 1999
Neuropathological features of frontotemporal dementia and parkinsonism linked to chromosome 17q21-22 (FTDP-17): Duke Family 1684
C M Hulette, M A Pericak-Vance, A D Roses, et al.
Neuroscience Letters
|
August 11, 1998
No association of alpha1-antichymotrypsin flanking region polymorphism and Alzheimer disease risk in early- and late-onset Alzheimer disease patients
M P Bass, L H Yamaoka, W K Scott, et al.
American Journal of Medical Genetics
|
August 14, 1995
Confirmation of locus heterogeneity in the pure form of familial spastic paraplegia
M C Speer, H M Kingston, R M Boustany, et al.
Neuroscience Letters
|
April 22, 2005
An autosomal genomic screen for dementia in an extended Amish family
A E Ashley-Koch, Y Shao, J B Rimmler, et al.
Annals of Neurology
|
November 1, 1996
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13
J M Stajich, J M Gilchrist, F Lennon, et al.
Page
of 7