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Journal of Medical Genetics|June 1, 1980
A digitopalatal syndrome with associated anomalies of the heart, face, and skeletonR E Stevenson, H A Taylor, O M Burton, et al.The American Journal of Cardiology|November 17, 1998
Management and outcomes for black patients with acute myocardial infarction in the reperfusion era. National Registry of Myocardial Infarction 2 InvestigatorsH A Taylor, J G Canto, B Sanderson, et al.American Journal of Epidemiology|October 24, 1998
Ethnic disparities in patient recall of physician recommendations of diagnostic and treatment procedures for coronary diseaseB K Sanderson, J M Raczynski, C E Cornell, et al.Canadian Journal of Experimental Psychology = Revue Canadienne De Psychologie Experimentale|July 4, 2001
Is the donut in front of the car? An electrophysiological study examining spatial reference frame processingH A Taylor, R R Faust, T Sitnikova, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|February 22, 1975
Mannosidosis: deficiency of a specific alpha-mannosidase component in cultured fibroblastsH A Taylor, G H Thomas, A Aylsworth, et al.Archives of Internal Medicine|February 13, 1995
Race and sex differences in rates of invasive cardiac procedures in US hospitals. Data from the National Hospital Discharge SurveyW H Giles, R F Anda, M L Casper, et al.American Journal of Medical Genetics|June 19, 1998
Constitutional del(19)(q12q13.1) in a three-year-old girl with severe phenotypic abnormalities affecting multiple organ systemsA S Kulharya, R C Michaelis, K S Norris, et al.Cytogenetics and Cell Genetics|January 1, 1991
Deletion mapping of plasminogen activator inhibitor, type I (PLANH1) and beta-glucuronidase (GUSB) in 7q21----q22C E Schwartz, P Stanislovitis, M C Phelan, et al.The American Journal of Cardiology|November 17, 1998
Presenting characteristics, treatment patterns, and clinical outcomes of non-black minorities in the National Registry of Myocardial Infarction 2J G Canto, H A Taylor, W J Rogers, et al.Journal of Child Neurology|June 1, 1997
beta-Galactosidase gene mutations in patients with slowly progressive GM1 gangliosidosisE M Kaye, C Shalish, J Livermore, et al.Pageof 6