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Neurology|May 16, 2002
Generalized epilepsy with febrile seizures plus: mutation of the sodium channel subunit SCN1BR H Wallace, I E Scheffer, G Parasivam, et al.
Medical Progress Through Technology|January 1, 1990
The design, construction and clinical evaluation of a small phased array transducer for intraoperative echocardiographyP Brommersma, J H Smyllie, L A van Herwerden, et al.
The Journal of Biological Chemistry|March 30, 2001
Identification of a novel human tankyrase through its interaction with the adaptor protein Grb14R J Lyons, R Deane, D K Lynch, et al.
Nature Genetics|August 1, 1992
Fragile X syndrome without CCG amplification has an FMR1 deletionA K Gedeon, E Baker, H Robinson, et al.
Nature Genetics|December 1, 1995
Cloning of the sulphamidase gene and identification of mutations in Sanfilippo A syndromeH S Scott, L Blanch, X H Guo, et al.
Cytogenetics and Cell Genetics|January 1, 1988
Human prostate-specific antigen (APS) is a member of the glandular kallikrein gene family at 19q13G R Sutherland, E Baker, V J Hyland, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|November 1, 1990
Quantitative echocardiographic analysis of global and regional left ventricular function: a problem revisitedP E Assmann, C J Slager, S G van der Borden, et al.
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