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L P Ranum

Showing results (11-20 of 26) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|September 1, 1989
Isolation and characterization of the nitrate reductase structural gene of Chlamydomonas reinhardtiiE Fernández, R Schnell, L P Ranum, et al.
Nature Genetics|November 1, 1993
Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type IM Y Chung, L P Ranum, L A Duvick, et al.
American Journal of Human Genetics|July 1, 1991
Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6pL P Ranum, L A Duvick, S S Rich, et al.
Human Molecular Genetics|August 25, 2000
SCA8 CTG repeat: en masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetranceM L Moseley, L J Schut, T D Bird, et al.
Human Molecular Genetics|August 11, 1999
Nuclear localization of the spinocerebellar ataxia type 7 protein, ataxin-7M D Kaytor, L A Duvick, P J Skinner, et al.
Nature Genetics|January 13, 1998
Rapid cloning of expanded trinucleotide repeat sequences from genomic DNAM D Koob, K A Benzow, T D Bird, et al.
Neurology|November 24, 1999
A nonpathogenic GAAGGA repeat in the Friedreich gene: implications for pathogenesisK Ohshima, N Sakamoto, M Labuda, et al.
Nature Genetics|April 7, 1999
An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)M D Koob, M L Moseley, L J Schut, et al.
Human Molecular Genetics|August 1, 2000
CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2)S Hayes, G Turecki, K Brisebois, et al.
Science (New York, N.Y.)|August 4, 2001
Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9C L Liquori, K Ricker, M L Moseley, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1989
Isolation and characterization of the nitrate reductase structural gene of Chlamydomonas reinhardtiiE Fernández, R Schnell, L P Ranum, et al.
Nature Genetics|November 1, 1993
Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type IM Y Chung, L P Ranum, L A Duvick, et al.
American Journal of Human Genetics|July 1, 1991
Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6pL P Ranum, L A Duvick, S S Rich, et al.
Human Molecular Genetics|August 25, 2000
SCA8 CTG repeat: en masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetranceM L Moseley, L J Schut, T D Bird, et al.
Human Molecular Genetics|August 11, 1999
Nuclear localization of the spinocerebellar ataxia type 7 protein, ataxin-7M D Kaytor, L A Duvick, P J Skinner, et al.
Nature Genetics|January 13, 1998
Rapid cloning of expanded trinucleotide repeat sequences from genomic DNAM D Koob, K A Benzow, T D Bird, et al.
Neurology|November 24, 1999
A nonpathogenic GAAGGA repeat in the Friedreich gene: implications for pathogenesisK Ohshima, N Sakamoto, M Labuda, et al.
Nature Genetics|April 7, 1999
An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)M D Koob, M L Moseley, L J Schut, et al.
Human Molecular Genetics|August 1, 2000
CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2)S Hayes, G Turecki, K Brisebois, et al.
Science (New York, N.Y.)|August 4, 2001
Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9C L Liquori, K Ricker, M L Moseley, et al.
Pageof 3