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Showing results (51-60 of 55) with videos related to

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Neuron|November 1, 1993
Huntington's disease gene (IT15) is widely expressed in human and rat tissuesS H Li, G Schilling, W S Young, et al.
American Journal of Medical Genetics|July 13, 2001
Familial influence on age of onset among siblings with Huntington diseaseA Rosenblatt, R R Brinkman, K Y Liang, 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 pedigreesM W Becher, D C Rubinsztein, J Leggo, et al.
Neurology|July 23, 1998
Patients with features similar to Huntington's disease, without CAG expansion in huntingtinA Rosenblatt, N G Ranen, D C Rubinsztein, 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 repeatsD C Rubinsztein, J Leggo, R Coles, et al.
Pageof 6

Showing results (51-60 of 55) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 55 results.
Neuron|November 1, 1993
Huntington's disease gene (IT15) is widely expressed in human and rat tissuesS H Li, G Schilling, W S Young, et al.
American Journal of Medical Genetics|July 13, 2001
Familial influence on age of onset among siblings with Huntington diseaseA Rosenblatt, R R Brinkman, K Y Liang, 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 pedigreesM W Becher, D C Rubinsztein, J Leggo, et al.
Neurology|July 23, 1998
Patients with features similar to Huntington's disease, without CAG expansion in huntingtinA Rosenblatt, N G Ranen, D C Rubinsztein, 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 repeatsD C Rubinsztein, J Leggo, R Coles, et al.
Pageof 6