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Genomics
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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.
Neurology
|
March 12, 2003
Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease
T Foroud, S K Uniacke, L Liu, et al.
Genomics
|
January 1, 1989
A genetic linkage map of the long arm of human chromosome 22
G A Rouleau, J L Haines, A Bazanowski, 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.
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 19
D L Koller, K E White, G Liu, et al.
Birth Defects Original Article Series
|
January 1, 1975
Linkage group I: multipoint mapping
D A Meyers, P M Conneally, F Hecht, et al.
Cytogenetics and Cell Genetics
|
January 1, 1975
Linkage relationships of 1qh to Amy, Fy, PGM1, and Rh
M L Rivas, P M Conneally, F Hecht, et al.
JAMA
|
July 11, 1977
Cooperative study of hospital frequency and character of transient ischemic attacks. III. Variations in treatment
A F Haerer, R A Gotshall, P M Conneally, 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 locus
I Takacs, D L Koller, M Peacock, et al.
Page
of 19
Search research articles
Search
Showing results (111-120 of 186) with videos related to
Sort By:
Page
of 19
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.
Neurology
|
March 12, 2003
Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease
T Foroud, S K Uniacke, L Liu, et al.
Genomics
|
January 1, 1989
A genetic linkage map of the long arm of human chromosome 22
G A Rouleau, J L Haines, A Bazanowski, 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.
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 19
D L Koller, K E White, G Liu, et al.
Birth Defects Original Article Series
|
January 1, 1975
Linkage group I: multipoint mapping
D A Meyers, P M Conneally, F Hecht, et al.
Cytogenetics and Cell Genetics
|
January 1, 1975
Linkage relationships of 1qh to Amy, Fy, PGM1, and Rh
M L Rivas, P M Conneally, F Hecht, et al.
JAMA
|
July 11, 1977
Cooperative study of hospital frequency and character of transient ischemic attacks. III. Variations in treatment
A F Haerer, R A Gotshall, P M Conneally, 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 locus
I Takacs, D L Koller, M Peacock, et al.
Page
of 19