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The Journal of Clinical Investigation|September 1, 1989
Clustering of multiallele DNA markers near the Huntington's disease geneM E MacDonald, S V Cheng, M Zimmer, et al.
The American Surgeon|July 28, 2026
When Lockdowns Were Not Equal: State COVID-19 Policies and Firearm Mortality Across Demographic GroupsWilliam M Rice, Asad H Khan, Jack Otterson, et al.
Investigative Ophthalmology & Visual Science|July 13, 2014
Set-based joint test of interaction between SNPs in the VEGF pathway and exogenous estrogen finds association with age-related macular degenerationMonique D Courtenay, William Cade, Stephen G Schwartz, et al.
Clinical Nutrition ESPEN|July 25, 2022
Micronutrient deficiencies in critically ill patients receiving continuous renal replacement therapyMegan Fah, Laura E Van Althuis, Tetsu Ohnuma, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Genetic heterogeneity in tuberous sclerosis. Study of a large collaborative datasetJ L Haines, J Amos, J Attwood, et al.
Annals of Neurology|June 1, 1996
Alzheimer's disease and apolipoprotein E-4 allele in an Amish populationM A Pericak-Vance, C C Johnson, J B Rimmler, et al.
Neuron|August 1, 1989
Recombination events suggest potential sites for the Huntington's disease geneM E MacDonald, J L Haines, M Zimmer, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 24, 2025
Basic Science and PathogenesisRazaq O Durodoye, Timothy H Ciesielski, Penelope Benchek, et al.
American Journal of Human Genetics|April 28, 2001
A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tardaG E Tiller, V L Hannig, D Dozier, et al.
Advances in Experimental Medicine and Biology|July 13, 2023
Integrating Computational Approaches to Predict the Effect of Genetic Variants on Protein Stability in Retinal Degenerative DiseaseMichelle Grunin, Ellen Palmer, Sarah de Jong, et al.
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