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Journal of Medical Genetics
|
December 1, 1985
Genetic linkage between Huntington's disease and the DNA polymorphism G8 in South Wales families
P S Harper, S Youngman, M A Anderson, et al.
Birth Defects Original Article Series
|
January 11, 1975
Linkage relations of the loci for the MN blood group and red cell acid phosphatase
L R Weitkamp, E W Lovrien, B Olaisen, 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.
Neurology
|
November 1, 1989
Gerstmann-Sträussler-Scheinker disease. II. Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected family
B Ghetti, F Tagliavini, C L Masters, et al.
Journal of Medical Genetics
|
December 1, 1993
Gametic but not somatic instability of CAG repeat length in Huntington's disease
M E MacDonald, G Barnes, J Srinidhi, 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.
Cold Spring Harbor Symposia on Quantitative Biology
|
January 1, 1986
Molecular genetics of Huntington's disease
J F Gusella, T C Gilliam, R E Tanzi, et al.
Annals of the New York Academy of Sciences
|
January 1, 1991
Genetic heterogeneity in tuberous sclerosis. Study of a large collaborative dataset
J L Haines, J Amos, J Attwood, et al.
Somatic Cell and Molecular Genetics
|
January 1, 1993
A genetic linkage map of the chromosome 4 short arm
P A Locke, M E MacDonald, J Srinidhi, et al.
JAMA
|
November 28, 1977
Cooperative study of hospital frequency and character of transient ischemic attacks. V. Symptom analysis
D E Futty, M Conneally, M L Dyken, et al.
Page
of 20
Search research articles
Search
Showing results (131-140 of 194) with videos related to
Sort By:
Page
of 20
Journal of Medical Genetics
|
December 1, 1985
Genetic linkage between Huntington's disease and the DNA polymorphism G8 in South Wales families
P S Harper, S Youngman, M A Anderson, et al.
Birth Defects Original Article Series
|
January 11, 1975
Linkage relations of the loci for the MN blood group and red cell acid phosphatase
L R Weitkamp, E W Lovrien, B Olaisen, 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.
Neurology
|
November 1, 1989
Gerstmann-Sträussler-Scheinker disease. II. Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected family
B Ghetti, F Tagliavini, C L Masters, et al.
Journal of Medical Genetics
|
December 1, 1993
Gametic but not somatic instability of CAG repeat length in Huntington's disease
M E MacDonald, G Barnes, J Srinidhi, 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.
Cold Spring Harbor Symposia on Quantitative Biology
|
January 1, 1986
Molecular genetics of Huntington's disease
J F Gusella, T C Gilliam, R E Tanzi, et al.
Annals of the New York Academy of Sciences
|
January 1, 1991
Genetic heterogeneity in tuberous sclerosis. Study of a large collaborative dataset
J L Haines, J Amos, J Attwood, et al.
Somatic Cell and Molecular Genetics
|
January 1, 1993
A genetic linkage map of the chromosome 4 short arm
P A Locke, M E MacDonald, J Srinidhi, et al.
JAMA
|
November 28, 1977
Cooperative study of hospital frequency and character of transient ischemic attacks. V. Symptom analysis
D E Futty, M Conneally, M L Dyken, et al.
Page
of 20