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J Buckle

Showing results (91-100 of 137) with videos related to

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Journal of the Neurological Sciences|January 31, 2009
Spinal cord lesions and clinical status in multiple sclerosis: A 1.5 T and 3 T MRI studyJ M Stankiewicz, M Neema, D C Alsop, et al.
Lancet (London, England)|October 7, 1989
Detection of breakpoints in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic diseaseJ Lamb, A O Wilkie, P C Harris, et al.
American Journal of Medical Genetics|January 30, 1995
Clinical and hematologic aspects of the X-linked alpha-thalassemia/mental retardation syndrome (ATR-X)R J Gibbons, L Brueton, V J Buckle, et al.
Cell|February 8, 1991
Stable length polymorphism of up to 260 kb at the tip of the short arm of human chromosome 16A O Wilkie, D R Higgs, K A Rack, et al.
Neurology|September 17, 2008
CTLA4Ig treatment in patients with multiple sclerosis: an open-label, phase 1 clinical trialV Viglietta, K Bourcier, G J Buckle, et al.
Human Molecular Genetics|February 7, 2001
Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16R J Daniels, J F Peden, C Lloyd, et al.
Blood|July 1, 1990
Alpha-thalassemia caused by a large (62 kb) deletion upstream of the human alpha globin gene clusterC S Hatton, A O Wilkie, H C Drysdale, et al.
Science Translational Medicine|September 29, 2012
An RNA profile identifies two subsets of multiple sclerosis patients differing in disease activityLinda Ottoboni, Brendan T Keenan, Pablo Tamayo, et al.
American Journal of Human Genetics|June 1, 1990
Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3A O Wilkie, V J Buckle, P C Harris, et al.
The Journal of Biological Chemistry|October 12, 2000
Relationship between novel isoforms, functionally important domains, and subcellular distribution of CD164/endolynJ Y Chan, J E Lee-Prudhoe, B Jorgensen, et al.
Pageof 14

Showing results (91-100 of 137) with videos related to

Sort By:
Pageof 14
Journal of the Neurological Sciences|January 31, 2009
Spinal cord lesions and clinical status in multiple sclerosis: A 1.5 T and 3 T MRI studyJ M Stankiewicz, M Neema, D C Alsop, et al.
Lancet (London, England)|October 7, 1989
Detection of breakpoints in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic diseaseJ Lamb, A O Wilkie, P C Harris, et al.
American Journal of Medical Genetics|January 30, 1995
Clinical and hematologic aspects of the X-linked alpha-thalassemia/mental retardation syndrome (ATR-X)R J Gibbons, L Brueton, V J Buckle, et al.
Cell|February 8, 1991
Stable length polymorphism of up to 260 kb at the tip of the short arm of human chromosome 16A O Wilkie, D R Higgs, K A Rack, et al.
Neurology|September 17, 2008
CTLA4Ig treatment in patients with multiple sclerosis: an open-label, phase 1 clinical trialV Viglietta, K Bourcier, G J Buckle, et al.
Human Molecular Genetics|February 7, 2001
Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16R J Daniels, J F Peden, C Lloyd, et al.
Blood|July 1, 1990
Alpha-thalassemia caused by a large (62 kb) deletion upstream of the human alpha globin gene clusterC S Hatton, A O Wilkie, H C Drysdale, et al.
Science Translational Medicine|September 29, 2012
An RNA profile identifies two subsets of multiple sclerosis patients differing in disease activityLinda Ottoboni, Brendan T Keenan, Pablo Tamayo, et al.
American Journal of Human Genetics|June 1, 1990
Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3A O Wilkie, V J Buckle, P C Harris, et al.
The Journal of Biological Chemistry|October 12, 2000
Relationship between novel isoforms, functionally important domains, and subcellular distribution of CD164/endolynJ Y Chan, J E Lee-Prudhoe, B Jorgensen, et al.
Pageof 14