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Molecular Microbiology|August 5, 2017
Bacillus subtilis genome project: cloning and sequencing of the 97 kb region from 325° to 333degP Glaser, F Kunst, M Arnaud, et al.Journal of the National Comprehensive Cancer Network : JNCCN|February 16, 2026
A Taxonomy for Assessing Real-World Targeted Cancer Therapy Options in the Context of Broad Genomic ProfilingXiao Wang, Jessica B Long, John Rothen, et al.Diabetologia|September 10, 2008
Socioeconomic inequalities in diabetes mellitus across Europe at the beginning of the 21st centuryA Espelt, C Borrell, A J Roskam, et al.Hearing Research|July 17, 2012
Audiometric characteristics of two Dutch families with non-ocular Stickler syndrome (COL11A2)E van Beelen, J M Leijendeckers, P L M Huygen, et al.Journal of Medical Genetics|July 29, 1999
A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locusG Van Camp, H Kunst, K Flothmann, et al.Hearing Research|January 24, 2013
Progressive hereditary hearing impairment caused by a MYO6 mutation resembles presbyacusisA M M Oonk, J M Leijendeckers, E M Lammers, et al.Journal of Laboratory Automation|January 17, 2013
cobas 8000 Modular analyzer series evaluated under routine-like conditions at 14 sites in Australia, Europe, and the United StatesArnold von Eckardstein, Hans Jürgen Roth, Graham Jones, et al.Drug and Alcohol Dependence|August 19, 2015
Trends and socioeconomic differences in policy triggers for thinking about quitting smoking: Findings from the International Tobacco Control (ITC) Europe SurveysKarin Hummel, Gera E Nagelhout, Marc C Willemsen, et al.Journal of Clinical Microbiology|July 16, 2020
Evaluation of Six Commercial Mid- to High-Volume Antibody and Six Point-of-Care Lateral Flow Assays for Detection of SARS-CoV-2 AntibodiesCarmen L Charlton, Jamil N Kanji, Kam Johal, et al.Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 12, 2021
A Novel COCH Mutation Affects the vWFA2 Domain and Leads to a Relatively Mild DFNA9 PhenotypeJeroen J Smits, Eline van Beelen, Nicole J D Weegerink, et al.Pageof 151