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Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2003
Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probandsArti Pandya, Kathleen S Arnos, Xia J Xia, et al.
JAMA Pediatrics|January 13, 2015
Evaluation of the effect of human immunodeficiency virus-related structural interventions: the connect to protect projectJonathan M Ellen, Lauren Greenberg, Nancy Willard, et al.
Journal of Medical Genetics|March 25, 2018
Inframe deletion of human ESPN is associated with deafness, vestibulopathy and vision impairmentZubair M Ahmed, Thomas J Jaworek, Gowri N Sarangdhar, et al.
The Journal of Biological Chemistry|February 8, 2007
Deafness and stria vascularis defects in S1P2 receptor-null miceMari Kono, Inna A Belyantseva, Athanasia Skoura, et al.
The American Journal of Cardiology|May 21, 2005
Antianginal efficacy of omapatrilat in patients with chronic angina pectorisBernard R Chaitman, Alla Y Ivleva, Marek Ujda, et al.
European Journal of Human Genetics : EJHG|July 16, 2009
DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3Shahid Yar Khan, Saima Riazuddin, Mohsin Shahzad, et al.
Pediatric Research|March 19, 2004
The R245X mutation of PCDH15 in Ashkenazi Jewish children diagnosed with nonsyndromic hearing loss foreshadows retinitis pigmentosaZippora Brownstein, Tamar Ben-Yosef, Orit Dagan, et al.
Human Genetics|July 7, 2021
Human deafness-associated variants alter the dynamics of key molecules in hair cell stereocilia F-actin coresTakushi Miyoshi, Inna A Belyantseva, Shin-Ichiro Kitajiri, et al.
BMC Medical Genetics|February 11, 2011
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndromeSaima Riazuddin, Zubair M Ahmed, Rashmi S Hegde, et al.
Alimentary Pharmacology & Therapeutics|February 23, 2018
Randomised clinical trial: efficacy, safety and dosage of adjunctive allopurinol in azathioprine/mercaptopurine nonresponders (AAA Study)A B Friedman, S J Brown, P Bampton, et al.
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