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Science (New York, N.Y.)
|
December 8, 1989
A new DNA marker tightly linked to the fragile X locus (FRAXA)
G K Suthers, D F Callen, V J Hyland, et al.
Science (New York, N.Y.)
|
November 4, 1988
Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy
S B Malhotra, K A Hart, H J Klamut, et al.
American Journal of Human Genetics
|
April 11, 2001
Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14
M McEntagart, N Norton, H Williams, et al.
Genomics
|
August 1, 1989
Huntington disease: no evidence for locus heterogeneity
P M Conneally, J L Haines, R E Tanzi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 1, 1997
Dentatorubral and pallidoluysian atrophy (DRPLA). Clinical and neuropathological findings in genetically confirmed North American and European pedigrees
M W Becher, D C Rubinsztein, J Leggo, et al.
American Journal of Human Genetics
|
July 1, 1996
Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats
D C Rubinsztein, J Leggo, R Coles, et al.
Page
of 22
Search research articles
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Showing results (211-220 of 216) with videos related to
Sort By:
Page
of 22
You have reached the last page of results.
This site can display upto 216 results.
Science (New York, N.Y.)
|
December 8, 1989
A new DNA marker tightly linked to the fragile X locus (FRAXA)
G K Suthers, D F Callen, V J Hyland, et al.
Science (New York, N.Y.)
|
November 4, 1988
Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy
S B Malhotra, K A Hart, H J Klamut, et al.
American Journal of Human Genetics
|
April 11, 2001
Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14
M McEntagart, N Norton, H Williams, et al.
Genomics
|
August 1, 1989
Huntington disease: no evidence for locus heterogeneity
P M Conneally, J L Haines, R E Tanzi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 1, 1997
Dentatorubral and pallidoluysian atrophy (DRPLA). Clinical and neuropathological findings in genetically confirmed North American and European pedigrees
M W Becher, D C Rubinsztein, J Leggo, et al.
American Journal of Human Genetics
|
July 1, 1996
Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats
D C Rubinsztein, J Leggo, R Coles, et al.
Page
of 22