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S-M Pulst

Showing results (91-100 of 106) with videos related to

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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.
Neurology|June 1, 1996
Genetic mapping of the spinocerebellar ataxia type 2 gene on human chromosome 12A Nechiporuk, I Lopes-Cendes, T Nechiporuk, et al.
Genomics|November 5, 1997
A high-resolution PAC and BAC map of the SCA2 regionT Nechiporuk, A Nechiporuk, S Sahba, et al.
Human Genetics|April 1, 1996
Identification of three new microsatellite markers in the spinocerebellar ataxia type 2 (SCA2) region and 1.2 Mb physical mapT Nechiporuk, A Nechiporuk, X Guan, et al.
Neurology|September 2, 2005
An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?M F Waters, D Fee, K P Figueroa, et al.
American Journal of Human Genetics|August 1, 1990
Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotypeJ R Korenberg, H Kawashima, S M Pulst, et al.
American Journal of Human Genetics|November 1, 1992
Linkage and mutational analysis of familial Alzheimer disease kindreds for the APP gene regionK Kamino, H T Orr, H Payami, et al.
American Journal of Medical Genetics|January 1, 1992
Stable ring chromosome 21: molecular and clinical definition of the lesionT C Falik-Borenstein, T M Pribyl, S M Pulst, et al.
Archives of Neurology|October 6, 1997
Spinocerebellar ataxia type 2. Genotype and phenotype in German kindredsL Schöls, S Gispert, M Vorgerd, et al.
Human Molecular Genetics|October 16, 1999
Analysis of the dynamic mutation in the SCA7 gene shows marked parental effects on CAG repeat transmissionL G Gouw, M A Castañeda, C K McKenna, et al.
Pageof 11

Showing results (91-100 of 106) with videos related to

Sort By:
Pageof 11
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.
Neurology|June 1, 1996
Genetic mapping of the spinocerebellar ataxia type 2 gene on human chromosome 12A Nechiporuk, I Lopes-Cendes, T Nechiporuk, et al.
Genomics|November 5, 1997
A high-resolution PAC and BAC map of the SCA2 regionT Nechiporuk, A Nechiporuk, S Sahba, et al.
Human Genetics|April 1, 1996
Identification of three new microsatellite markers in the spinocerebellar ataxia type 2 (SCA2) region and 1.2 Mb physical mapT Nechiporuk, A Nechiporuk, X Guan, et al.
Neurology|September 2, 2005
An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?M F Waters, D Fee, K P Figueroa, et al.
American Journal of Human Genetics|August 1, 1990
Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotypeJ R Korenberg, H Kawashima, S M Pulst, et al.
American Journal of Human Genetics|November 1, 1992
Linkage and mutational analysis of familial Alzheimer disease kindreds for the APP gene regionK Kamino, H T Orr, H Payami, et al.
American Journal of Medical Genetics|January 1, 1992
Stable ring chromosome 21: molecular and clinical definition of the lesionT C Falik-Borenstein, T M Pribyl, S M Pulst, et al.
Archives of Neurology|October 6, 1997
Spinocerebellar ataxia type 2. Genotype and phenotype in German kindredsL Schöls, S Gispert, M Vorgerd, et al.
Human Molecular Genetics|October 16, 1999
Analysis of the dynamic mutation in the SCA7 gene shows marked parental effects on CAG repeat transmissionL G Gouw, M A Castañeda, C K McKenna, et al.
Pageof 11