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D C Rubinsztein

Showing results (61-70 of 125) with videos related to

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European Journal of Human Genetics : EJHG|January 1, 1994
The EUROGEM map of human chromosome 9J Attwood, G Vergnaud, M L Lush, et al.
American Journal of Medical Genetics|February 25, 2000
Genetic associations with clinical characteristics in bipolar affective disorder and recurrent unipolar depressive disorderL W Ho, R A Furlong, J S Rubinsztein, et al.
American Journal of Human Genetics|September 16, 1999
An empirical exploration of the (delta mu)2 genetic distance for 213 human microsatellite markersG Cooper, W Amos, R Bellamy, et al.
Human Molecular Genetics|September 1, 1995
Sequence variation and size ranges of CAG repeats in the Machado-Joseph disease, spinocerebellar ataxia type 1 and androgen receptor genesD C Rubinsztein, J Leggo, G A Coetzee, et al.
Journal of Medical Genetics|December 1, 1996
The tRNA(Gln) 4336 mitochondrial DNA variant is not a high penetrance mutation which predisposes to dementia before the age of 75 yearsC Tysoe, D Robinson, C Brayne, et al.
Neurology|September 26, 1997
Homozygotes and heterozygotes for ciliary neurotrophic factor null alleles do not show earlier onset of Huntington's diseaseD C Rubinsztein, J Leggo, M Chiano, et al.
Journal of Medical Genetics|January 16, 1998
Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UKJ Leggo, A Dalton, P J Morrison, et al.
Journal of Medical Genetics|September 10, 2003
Meta-analysis of age at onset in spastin-associated hereditary spastic paraplegia provides no evidence for a correlation with mutational classA G Yip, A Dürr, D A Marchuk, et al.
American Journal of Medical Genetics|September 20, 1996
Analysis of polyglutamine-coding repeats in the TATA-binding protein in different human populations and in patients with schizophrenia and bipolar affective disorderD C Rubinsztein, J Leggo, T J Crow, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|July 1, 1993
Characterization of six patients who are double heterozygotes for familial hypercholesterolemia and familial defective apo B-100D C Rubinsztein, F J Raal, H C Seftel, et al.
Pageof 13

Showing results (61-70 of 125) with videos related to

Sort By:
Pageof 13
European Journal of Human Genetics : EJHG|January 1, 1994
The EUROGEM map of human chromosome 9J Attwood, G Vergnaud, M L Lush, et al.
American Journal of Medical Genetics|February 25, 2000
Genetic associations with clinical characteristics in bipolar affective disorder and recurrent unipolar depressive disorderL W Ho, R A Furlong, J S Rubinsztein, et al.
American Journal of Human Genetics|September 16, 1999
An empirical exploration of the (delta mu)2 genetic distance for 213 human microsatellite markersG Cooper, W Amos, R Bellamy, et al.
Human Molecular Genetics|September 1, 1995
Sequence variation and size ranges of CAG repeats in the Machado-Joseph disease, spinocerebellar ataxia type 1 and androgen receptor genesD C Rubinsztein, J Leggo, G A Coetzee, et al.
Journal of Medical Genetics|December 1, 1996
The tRNA(Gln) 4336 mitochondrial DNA variant is not a high penetrance mutation which predisposes to dementia before the age of 75 yearsC Tysoe, D Robinson, C Brayne, et al.
Neurology|September 26, 1997
Homozygotes and heterozygotes for ciliary neurotrophic factor null alleles do not show earlier onset of Huntington's diseaseD C Rubinsztein, J Leggo, M Chiano, et al.
Journal of Medical Genetics|January 16, 1998
Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UKJ Leggo, A Dalton, P J Morrison, et al.
Journal of Medical Genetics|September 10, 2003
Meta-analysis of age at onset in spastin-associated hereditary spastic paraplegia provides no evidence for a correlation with mutational classA G Yip, A Dürr, D A Marchuk, et al.
American Journal of Medical Genetics|September 20, 1996
Analysis of polyglutamine-coding repeats in the TATA-binding protein in different human populations and in patients with schizophrenia and bipolar affective disorderD C Rubinsztein, J Leggo, T J Crow, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|July 1, 1993
Characterization of six patients who are double heterozygotes for familial hypercholesterolemia and familial defective apo B-100D C Rubinsztein, F J Raal, H C Seftel, et al.
Pageof 13