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JMIR Bioinformatics and Biotechnology|April 14, 2026
The AudioGene Translational Dashboard for Diagnosing Autosomal Dominant Nonsyndromic Hearing Loss: Phenotypic Data Visualization and Analysis StudyBenjamin DeSollar, Nathan Schaefer, Daniel Walls, et al.Journal of Medical Genetics|January 20, 2004
A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3R L Snoeckx, H Kremer, R J H Ensink, et al.Blood|August 22, 2009
Chromosome looping at the human alpha-globin locus is mediated via the major upstream regulatory element (HS -40)Douglas Vernimmen, Fatima Marques-Kranc, Jacqueline A Sharpe, et al.BMC Nephrology|May 14, 2025
Pregnancy outcomes in C3 glomerulopathy: a retrospective reviewLauren O Fergus, Meryl Waldmann, Monica D Hall, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 30, 2013
C3 glomerulonephritis associated with monoclonal gammopathy: a case seriesLadan Zand, Andrea Kattah, Fernando C Fervenza, et al.Archives of Disease in Childhood|September 15, 2007
Infant HIV infection despite "universal" antenatal testingS S Struik, G Tudor-Williams, G P Taylor, et al.Journal of Medical Genetics|June 3, 2004
DFNA5: hearing impairment exon instead of hearing impairment gene?L Van Laer, K Vrijens, S Thys, et al.American Journal of Human Genetics|May 31, 2016
RNA Interference Prevents Autosomal-Dominant Hearing LossSeiji B Shibata, Paul T Ranum, Hideaki Moteki, et al.Journal of Medical Genetics|November 14, 2006
Sensorineural deafness and male infertility: a contiguous gene deletion syndromeYuzhou Zhang, Mahdi Malekpour, Navid Al-Madani, et al.Clinical Genetics|September 9, 2015
Comprehensive genetic testing with ethnic-specific filtering by allele frequency in a Japanese hearing-loss populationH Moteki, H Azaiez, K T Booth, et al.Pageof 71