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M H Abbott

Showing results (11-20 of 17) with videos related to

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Science (New York, N.Y.)|August 23, 1985
Huntington's disease: two families with differing clinical features show linkage to the G8 probeS E Folstein, J A Phillips, D A Meyers, et al.
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|January 1, 1997
Fine mapping of the nail-patella syndrome locus at 9q34I McIntosh, M V Clough, A A Schäffer, 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 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Science (New York, N.Y.)|August 23, 1985
Huntington's disease: two families with differing clinical features show linkage to the G8 probeS E Folstein, J A Phillips, D A Meyers, et al.
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|January 1, 1997
Fine mapping of the nail-patella syndrome locus at 9q34I McIntosh, M V Clough, A A Schäffer, 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 2