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K E Morrison

Showing results (21-30 of 47) with videos related to

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Human Molecular Genetics|October 1, 1993
Dinucleotide repeat polymorphism proximal to the spinal muscular atrophy region at D5S681K E Morrison, R J Daniels, L Campbell, et al.
Annals of Neurology|December 10, 1997
Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: analysis of 155 cases and identification of a novel insertion mutationM Jackson, A Al-Chalabi, Z E Enayat, et al.
Journal of Clinical Microbiology|January 5, 2000
Confirmation of psaA in all 90 serotypes of Streptococcus pneumoniae by PCR and potential of this assay for identification and diagnosisK E Morrison, D Lake, J Crook, et al.
Neurology|September 28, 2005
Association of the H63D polymorphism in the hemochromatosis gene with sporadic ALSE F Goodall, M J Greenway, I van Marion, et al.
Journal of Autoimmunity|April 1, 1996
Human muscle acetylcholine receptor alpha-subunit gene (CHRNA1) association with autoimmune myasthenia gravis in black, mixed-ancestry and Caucasian subjectsJ M Heckmann, K E Morrison, B Emeryk-Szajewska, et al.
Human Molecular Genetics|November 1, 1994
Cloning the shared components of complex DNA resourcesA J Brookes, E M Slorach, K E Morrison, et al.
Radiology|February 1, 1997
Malignant esophageal obstruction and esophagorespiratory fistula: palliation with a polyethylene-covered Z-stentR R Saxon, K E Morrison, P C Lakin, et al.
Neurochemistry International|June 16, 2011
Changes in iron-regulatory gene expression occur in human cell culture models of Parkinson's diseaseC B Carroll, M-L Zeissler, N Chadborn, et al.
American Journal of Human Genetics|March 1, 1992
High-resolution genetic map around the spinal muscular atrophy (SMA) locus on chromosome 5K E Morrison, R J Daniels, G K Suthers, et al.
BMC Genetics|July 15, 2015
Establishing the UK DNA Bank for motor neuron disease (MND)Lucy Smith, B C Cupid, B G M Dickie, et al.
Pageof 5

Showing results (21-30 of 47) with videos related to

Sort By:
Pageof 5
Human Molecular Genetics|October 1, 1993
Dinucleotide repeat polymorphism proximal to the spinal muscular atrophy region at D5S681K E Morrison, R J Daniels, L Campbell, et al.
Annals of Neurology|December 10, 1997
Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: analysis of 155 cases and identification of a novel insertion mutationM Jackson, A Al-Chalabi, Z E Enayat, et al.
Journal of Clinical Microbiology|January 5, 2000
Confirmation of psaA in all 90 serotypes of Streptococcus pneumoniae by PCR and potential of this assay for identification and diagnosisK E Morrison, D Lake, J Crook, et al.
Neurology|September 28, 2005
Association of the H63D polymorphism in the hemochromatosis gene with sporadic ALSE F Goodall, M J Greenway, I van Marion, et al.
Journal of Autoimmunity|April 1, 1996
Human muscle acetylcholine receptor alpha-subunit gene (CHRNA1) association with autoimmune myasthenia gravis in black, mixed-ancestry and Caucasian subjectsJ M Heckmann, K E Morrison, B Emeryk-Szajewska, et al.
Human Molecular Genetics|November 1, 1994
Cloning the shared components of complex DNA resourcesA J Brookes, E M Slorach, K E Morrison, et al.
Radiology|February 1, 1997
Malignant esophageal obstruction and esophagorespiratory fistula: palliation with a polyethylene-covered Z-stentR R Saxon, K E Morrison, P C Lakin, et al.
Neurochemistry International|June 16, 2011
Changes in iron-regulatory gene expression occur in human cell culture models of Parkinson's diseaseC B Carroll, M-L Zeissler, N Chadborn, et al.
American Journal of Human Genetics|March 1, 1992
High-resolution genetic map around the spinal muscular atrophy (SMA) locus on chromosome 5K E Morrison, R J Daniels, G K Suthers, et al.
BMC Genetics|July 15, 2015
Establishing the UK DNA Bank for motor neuron disease (MND)Lucy Smith, B C Cupid, B G M Dickie, et al.
Pageof 5