Showing results (511-520 of 704) with videos related to
Sort By:
Pageof 71
Journal of Human Genetics|April 12, 2007
A novel DFNA5 mutation does not cause hearing loss in an Iranian familyLut Van Laer, Nicole C Meyer, Mahdi Malekpour, et al.Human Mutation|April 15, 2014
TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing lossHela Azaiez, Kevin T Booth, Fengxiao Bu, et al.The Annals of Otology, Rhinology, and Laryngology|March 21, 2015
De novo mutation in X-linked hearing loss-associated POU3F4 in a sporadic case of congenital hearing lossHideaki Moteki, A Eliot Shearer, Shuji Izumi, et al.The Annals of Otology, Rhinology, and Laryngology|March 7, 2015
USH2 caused by GPR98 mutation diagnosed by massively parallel sequencing in advance of the occurrence of visual symptomsHideaki Moteki, Hidekane Yoshimura, Hela Azaiez, et al.Plos Genetics|August 22, 2009
A claudin-9-based ion permeability barrier is essential for hearingYoko Nakano, Sung H Kim, Hyoung-Mi Kim, et al.European Journal of Human Genetics : EJHG|July 22, 2010
Genetic male infertility and mutation of CATSPER ion channelsMichael S Hildebrand, Matthew R Avenarius, Marc Fellous, et al.Journal of Nephrology|July 19, 2015
C3 glomerulonephritis and autoimmune disease: more than a fortuitous association?Mariam P Alexander, Fernando C Fervenza, An S De Vriese, et al.Molecular Biology Reports|August 6, 2004
Refining the DFNB17 interval in consanguineous Indian familiesYingshi Guo, Valentina Pilipenko, Lynne H Y Lim, et al.Science (New York, N.Y.)|July 20, 2002
Impaired B and T cell antigen receptor signaling in p110delta PI 3-kinase mutant miceKlaus Okkenhaug, Antonio Bilancio, Géraldine Farjot, et al.Plos Genetics|November 11, 2011
Foxn1 regulates lineage progression in cortical and medullary thymic epithelial cells but is dispensable for medullary sublineage divergenceCraig S Nowell, Nicholas Bredenkamp, Stéphanie Tetélin, et al.Pageof 71