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Journal of Neuropathology and Experimental Neurology
|
July 1, 1997
In situ hybridization analysis of Girk2 expression in the developing central nervous system in normal and weaver mice
J Wei, S R Dlouhy, S Bayer, et al.
Genomics
|
August 1, 1992
Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15
K Young, T Foroud, P Williams, et al.
Archives of Neurology
|
June 1, 1996
Motor changes in presymptomatic Huntington disease gene carriers
E Siemers, T Foroud, D J Bill, et al.
Nature Genetics
|
April 1, 1992
Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene
S R Dlouhy, K Hsiao, M R Farlow, et al.
Nature Genetics
|
April 1, 1992
Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles
K Hsiao, S R Dlouhy, M R Farlow, et al.
Oncology
|
January 1, 1985
An amylase-producing serous cystadenocarcinoma of the ovary
M E Hodes, C J Sisk, R C Karn, et al.
Human Molecular Genetics
|
March 1, 1995
Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locus
V Allamand, O Broux, N Bourg, et al.
American Journal of Human Genetics
|
September 26, 2002
Genomic rearrangements resulting in PLP1 deletion occur by nonhomologous end joining and cause different dysmyelinating phenotypes in males and females
Ken Inoue, Hitoshi Osaka, Virginia C Thurston, et al.
American Journal of Medical Genetics
|
February 6, 1999
Different mutations in the same codon of the proteolipid protein gene, PLP, may help in correlating genotype with phenotype in Pelizaeus-Merzbacher disease/X-linked spastic paraplegia (PMD/SPG2)
M E Hodes, A W Zimmerman, A Aydanian, et al.
Annals of the New York Academy of Sciences
|
November 1, 2017
Peripheral Neuropathy Caused by Proteolipid Protein Gene Mutations
James Y Garbern, Franca Cambi, Richard Lewis, et al.
Page
of 15
Search research articles
Search
Showing results (131-140 of 144) with videos related to
Sort By:
Page
of 15
Journal of Neuropathology and Experimental Neurology
|
July 1, 1997
In situ hybridization analysis of Girk2 expression in the developing central nervous system in normal and weaver mice
J Wei, S R Dlouhy, S Bayer, et al.
Genomics
|
August 1, 1992
Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15
K Young, T Foroud, P Williams, et al.
Archives of Neurology
|
June 1, 1996
Motor changes in presymptomatic Huntington disease gene carriers
E Siemers, T Foroud, D J Bill, et al.
Nature Genetics
|
April 1, 1992
Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene
S R Dlouhy, K Hsiao, M R Farlow, et al.
Nature Genetics
|
April 1, 1992
Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles
K Hsiao, S R Dlouhy, M R Farlow, et al.
Oncology
|
January 1, 1985
An amylase-producing serous cystadenocarcinoma of the ovary
M E Hodes, C J Sisk, R C Karn, et al.
Human Molecular Genetics
|
March 1, 1995
Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locus
V Allamand, O Broux, N Bourg, et al.
American Journal of Human Genetics
|
September 26, 2002
Genomic rearrangements resulting in PLP1 deletion occur by nonhomologous end joining and cause different dysmyelinating phenotypes in males and females
Ken Inoue, Hitoshi Osaka, Virginia C Thurston, et al.
American Journal of Medical Genetics
|
February 6, 1999
Different mutations in the same codon of the proteolipid protein gene, PLP, may help in correlating genotype with phenotype in Pelizaeus-Merzbacher disease/X-linked spastic paraplegia (PMD/SPG2)
M E Hodes, A W Zimmerman, A Aydanian, et al.
Annals of the New York Academy of Sciences
|
November 1, 2017
Peripheral Neuropathy Caused by Proteolipid Protein Gene Mutations
James Y Garbern, Franca Cambi, Richard Lewis, et al.
Page
of 15