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L P Ranum

Showing results (21-30 of 26) with videos related to

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Genomics|December 1, 1993
Mapping and cloning of the critical region for the spinocerebellar ataxia type 1 gene (SCA1) in a yeast artificial chromosome contig spanning 1.2 MbS Banfi, M Y Chung, T J Kwiatkowski, et al.
American Journal of Human Genetics|September 1, 1995
Spinocerebellar ataxia type 1 and Machado-Joseph disease: incidence of CAG expansions among adult-onset ataxia patients from 311 families with dominant, recessive, or sporadic ataxiaL P Ranum, J K Lundgren, L J Schut, et al.
Neurology|February 1, 1992
Autosomal dominant spinocerebellar ataxia: locus heterogeneity in a Nebraska kindredL P Ranum, S S Rich, M A Nance, et al.
American Journal of Human Genetics|August 1, 1994
Molecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onsetL P Ranum, M Y Chung, S Banfi, et al.
Nature Genetics|July 1, 1993
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1H T Orr, M Y Chung, S Banfi, et al.
Neurology|December 17, 1998
Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia familiesM L Moseley, K A Benzow, L J Schut, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Genomics|December 1, 1993
Mapping and cloning of the critical region for the spinocerebellar ataxia type 1 gene (SCA1) in a yeast artificial chromosome contig spanning 1.2 MbS Banfi, M Y Chung, T J Kwiatkowski, et al.
American Journal of Human Genetics|September 1, 1995
Spinocerebellar ataxia type 1 and Machado-Joseph disease: incidence of CAG expansions among adult-onset ataxia patients from 311 families with dominant, recessive, or sporadic ataxiaL P Ranum, J K Lundgren, L J Schut, et al.
Neurology|February 1, 1992
Autosomal dominant spinocerebellar ataxia: locus heterogeneity in a Nebraska kindredL P Ranum, S S Rich, M A Nance, et al.
American Journal of Human Genetics|August 1, 1994
Molecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onsetL P Ranum, M Y Chung, S Banfi, et al.
Nature Genetics|July 1, 1993
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1H T Orr, M Y Chung, S Banfi, et al.
Neurology|December 17, 1998
Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia familiesM L Moseley, K A Benzow, L J Schut, et al.
Pageof 3