Showing results (271-280 of 282) with videos related to

Sort By:
Pageof 29
Journal of Medical Genetics|August 6, 2002
A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qterS H Blanton, C Y Liang, M W Cai, et al.
American Journal of Human Genetics|July 14, 2001
Two genes that map to the STSL locus cause sitosterolemia: genomic structure and spectrum of mutations involving sterolin-1 and sterolin-2, encoded by ABCG5 and ABCG8, respectivelyK Lu, M H Lee, S Hazard, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|May 21, 2023
Effect of the UNOS policy change on rates of rejection, infection, and hospital readmission following heart transplantationAjay S Vaidya, Emily S Lee, Eric S Kawaguchi, et al.
Critical Care Medicine|January 30, 2026
Recommendations for Advanced Practice Provider Postgraduate Training Programs in the United States: A Work Product of the Advanced Practice Provider Postgraduate Training Task Force of the Society of Critical Care MedicineDiane McLaughlin, Melissa Ricker, Aimee Abide, et al.
The Journal of Organic Chemistry|May 23, 2013
Synthesis of stereochemically and skeletally diverse fused ring systems from functionalized C-glycosidesBaudouin Gerard, Maurice D Lee, Sivaraman Dandapani, et al.
International Journal of Legal Medicine|January 1, 1997
Evaluation of Y-chromosomal STRs: a multicenter studyM Kayser, A Caglià, D Corach, et al.
Journal of Medical Genetics|April 5, 2003
Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafnessH-J Park, S Shaukat, X-Z Liu, et al.
Human Genetics|July 8, 1998
Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutationsA L DeStefano, L A Cupples, K S Arnos, et al.
International Journal of Legal Medicine|January 1, 1997
Chromosome Y microsatellites: population genetic and evolutionary aspectsP de Knijff, M Kayser, A Caglià, et al.
Clinical Genetics|March 19, 2010
A novel DFNB1 deletion allele supports the existence of a distant cis-regulatory region that controls GJB2 and GJB6 expressionE Wilch, H Azaiez, R A Fisher, et al.
Pageof 29