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BMC Medical Genetics|June 5, 2015
Novel compound heterozygous mutations in AMN cause Imerslund-Gräsbeck syndrome in two half-sisters: a case reportEmma Montgomery, John A Sayer, Laura A Baines, et al.
Psychiatric Services (Washington, D.C.)|February 19, 2014
Gender differences in VA disability status for PTSD over timeNina A Sayer, Emily M Hagel, Siamak Noorbaloochi, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|September 10, 2011
Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKDBodo B Beck, Howard Trachtman, Michael Gitman, et al.
BMC Developmental Biology|December 10, 2020
Expression patterns of ciliopathy genes ARL3 and CEP120 reveal roles in multisystem developmentL Powell, M Barroso-Gil, G J Clowry, et al.
European Geriatric Medicine|March 31, 2023
Using pre-fracture mobility to augment prediction of post-operative outcomes in hip fractureThomas A Stubbs, William J Doherty, Andrew Chaplin, et al.
Plos One|December 24, 2011
Clinical and functional characterization of URAT1 variantsVelibor Tasic, Ann Marie Hynes, Kenichiro Kitamura, et al.
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