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Journal of Medicine|January 1, 1984
Hematologic disorders and congenital cardiovascular malformations: converging lines of researchC Ferencz, J D Rubin, R J McCarter, et al.Teratology|June 1, 1987
Cardiac and noncardiac malformations: observations in a population-based studyC Ferencz, J D Rubin, R J McCarter, et al.The American Journal of Physiology|January 1, 1996
NHE2 and NHE3 are human and rabbit intestinal brush-border proteinsW A Hoogerwerf, S C Tsao, O Devuyst, et al.The American Journal of Physiology|June 1, 1996
Both the wild type and a functional isoform of CFTR are expressed in kidneyM M Morales, T P Carroll, T Morita, et al.Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|August 1, 1997
D2-like dopamine receptor density in Tourette syndrome measured by PETD F Wong, H S Singer, J Brandt, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 7, 2007
Multiple mitochondrial DNA deletions in monozygotic twins with OPMDM M K Muqit, A J Larner, M G Sweeney, et al.Journal of Toxicology and Environmental Health. Part A|November 4, 2008
Surveillance results of depleted uranium-exposed Gulf War I veterans: sixteen years of follow-upM A McDiarmid, S M Engelhardt, C D Dorsey, et al.Health Physics|June 15, 2007
Health surveillance of Gulf War I veterans exposed to depleted uranium: updating the cohortM A McDiarmid, S M Engelhardt, M Oliver, et al.Human Molecular Genetics|June 29, 2023
Multi-ancestry genome-wide analysis identifies shared genetic effects and common genetic variants for self-reported sleep durationB H Scammell, C Tchio, Y Song, et al.Neuromuscular Disorders : NMD|January 19, 2010
Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) geneHaiyan Zhou, Suzanne Lillis, Ryan E Loy, et al.Pageof 48