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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 Mb
S 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 ataxia
L P Ranum, J K Lundgren, L J Schut, et al.
Neurology
|
February 1, 1992
Autosomal dominant spinocerebellar ataxia: locus heterogeneity in a Nebraska kindred
L 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 onset
L 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 1
H T Orr, M Y Chung, S Banfi, et al.
Neurology
|
December 17, 1998
Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families
M L Moseley, K A Benzow, L J Schut, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 26) with videos related to
Sort By:
Page
of 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 Mb
S 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 ataxia
L P Ranum, J K Lundgren, L J Schut, et al.
Neurology
|
February 1, 1992
Autosomal dominant spinocerebellar ataxia: locus heterogeneity in a Nebraska kindred
L 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 onset
L 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 1
H T Orr, M Y Chung, S Banfi, et al.
Neurology
|
December 17, 1998
Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families
M L Moseley, K A Benzow, L J Schut, et al.
Page
of 3