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American Journal of Ophthalmology|June 15, 1991
The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutationN J Newman, M T Lott, D C Wallace
Revue Neurologique|January 1, 1991
MERRF: a model disease for understanding the principles of mitochondrial geneticsJ M Shoffner, M T Lott, D C Wallace
Biochemical and Biophysical Research Communications|September 30, 1988
Mitochondrial DNA in anucleate human blood cellsR C Shuster, A J Rubenstein, D C Wallace
Clinical Science (London, England : 1979)|September 1, 1987
Enhanced diurnal variation of blood pressure in the renal hypertensive rat: effect of angiotensin II suppressionE C Wallace, A J Balmforth, J J Morton
Somatic Cell Genetics|March 1, 1982
Assignment of an oligomycin-resistance locus to human chromosome 10K A Webster, N A Oliver, D C Wallace
Clinical and Experimental Rheumatology|August 29, 2003
Role of A-SAA in monitoring subclinical inflammation and in colchicine dosage in familial Mediterranean feverA Duzova, A Bakkaloglu, N Besbas, et al.
Clinical Rheumatology|October 25, 2003
The role of apoptosis in childhood Henoch-Schonlein purpuraF Ozaltin, N Besbas, D Uckan, et al.
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