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D A Stephenson

Showing results (41-50 of 49) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|January 1, 1991
Platelet-derived growth factor receptor alpha-subunit gene (Pdgfra) is deleted in the mouse patch (Ph) mutationD A Stephenson, M Mercola, E Anderson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 15, 2008
Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosumM-J Lee, T-W Cheng, M-S Hua, et al.
Genomics|August 1, 1989
Comparison of the physical and recombination maps of the mouse X chromosomeC M Disteche, G K McConnell, S G Grant, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 1, 1994
Mouse rump-white mutation associated with an inversion of chromosome 5D A Stephenson, K H Lee, D L Nagle, et al.
Annals of Human Genetics|March 30, 2000
Report and abstracts of the Sixth International Workshop on chromosome 9B P Chadwick, L J Campbell, C L Jackson, et al.
Annals of Human Genetics|July 17, 2008
HMBS mutations in Chinese patients with acute intermittent porphyriaC-C Yang, H-C Kuo, H-L You, et al.
Somatic Cell and Molecular Genetics|November 1, 1987
Regional localization of the murine Duchenne muscular dystrophy gene on the mouse X chromosomeJ S Chamberlain, S G Grant, A A Reeves, et al.
Neurology|August 13, 2008
SCA Functional Index: a useful compound performance measure for spinocerebellar ataxiaT Schmitz-Hübsch, P Giunti, D A Stephenson, et al.
Neurology|August 8, 2008
Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptomsT Schmitz-Hübsch, M Coudert, P Bauer, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1991
Platelet-derived growth factor receptor alpha-subunit gene (Pdgfra) is deleted in the mouse patch (Ph) mutationD A Stephenson, M Mercola, E Anderson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 15, 2008
Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosumM-J Lee, T-W Cheng, M-S Hua, et al.
Genomics|August 1, 1989
Comparison of the physical and recombination maps of the mouse X chromosomeC M Disteche, G K McConnell, S G Grant, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 1, 1994
Mouse rump-white mutation associated with an inversion of chromosome 5D A Stephenson, K H Lee, D L Nagle, et al.
Annals of Human Genetics|March 30, 2000
Report and abstracts of the Sixth International Workshop on chromosome 9B P Chadwick, L J Campbell, C L Jackson, et al.
Annals of Human Genetics|July 17, 2008
HMBS mutations in Chinese patients with acute intermittent porphyriaC-C Yang, H-C Kuo, H-L You, et al.
Somatic Cell and Molecular Genetics|November 1, 1987
Regional localization of the murine Duchenne muscular dystrophy gene on the mouse X chromosomeJ S Chamberlain, S G Grant, A A Reeves, et al.
Neurology|August 13, 2008
SCA Functional Index: a useful compound performance measure for spinocerebellar ataxiaT Schmitz-Hübsch, P Giunti, D A Stephenson, et al.
Neurology|August 8, 2008
Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptomsT Schmitz-Hübsch, M Coudert, P Bauer, et al.
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