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American Journal of Medical Genetics|September 19, 1997
SMN(T) and NAIP mutations in Canadian families with spinal muscular atrophy (SMA): genotype/phenotype correlations with disease severityL R Simard, C Rochette, A Semionov, et al.
Ophthalmology|October 1, 1985
Voluntary alteration of pattern visual evoked responsesR K Morgan, B Nugent, J M Harrison, et al.
American Journal of Medical Genetics|November 1, 1985
Hutterite cerebro-osteo-nephrodysplasia: autosomal recessive trait in a Lehrerleut Hutterite family from MontanaJ M Opitz, R B Lowry, T M Holmes, et al.
Neurosurgery|March 1, 1997
Chronic cerebral hypoperfusion: pathological and behavioral consequencesL H Sekhon, M K Morgan, I Spence, et al.
Antimicrobial Agents and Chemotherapy|October 8, 2008
Mechanisms accounting for fluoroquinolone resistance in Escherichia coli clinical isolatesSonia K Morgan-Linnell, Lauren Becnel Boyd, David Steffen, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|July 1, 1995
Familial cavernous angioma without clinical haemorrhageM J Day, M K Morgan, S C Wang, et al.
Annals of the Rheumatic Diseases|November 1, 1991
Absence of autoimmunity to type II collagen in generalised nodal osteoarthritisR B Clague, K Morgan, I Collins, et al.
Current Protocols in Pharmacology|September 28, 2011
Assessing sensitivity to antibacterial topoisomerase II inhibitorsSonia K Morgan-Linnell, Hiroshi Hiasa, Lynn Zechiedrich, et al.
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