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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2004 | 1 |
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PubMed for id: 463629
7 results
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Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss.
Gene. 2013 Aug 1;525(1):1-4. doi: 10.1016/j.gene.2013.04.078. Epub 2013 May 13.
Gene. 2013.
PMID: 23680645
USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1.
Jaworek TJ, Bhatti R, Latief N, Khan SN, Riazuddin S, Ahmed ZM.
Jaworek TJ, et al.
J Hum Genet. 2012 Oct;57(10):633-7. doi: 10.1038/jhg.2012.79. Epub 2012 Jun 21.
J Hum Genet. 2012.
PMID: 22718019
Free PMC article.
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Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families.
Shahin H, Walsh T, Rayyan AA, Lee MK, Higgins J, Dickel D, Lewis K, Thompson J, Baker C, Nord AS, Stray S, Gurwitz D, Avraham KB, King MC, Kanaan M.
Shahin H, et al.
Eur J Hum Genet. 2010 Apr;18(4):407-13. doi: 10.1038/ejhg.2009.190. Epub 2009 Nov 4.
Eur J Hum Genet. 2010.
PMID: 19888295
Free PMC article.
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Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans.
Grillet N, Schwander M, Hildebrand MS, Sczaniecka A, Kolatkar A, Velasco J, Webster JA, Kahrizi K, Najmabadi H, Kimberling WJ, Stephan D, Bahlo M, Wiltshire T, Tarantino LM, Kuhn P, Smith RJ, Müller U.
Grillet N, et al.
Am J Hum Genet. 2009 Sep;85(3):328-37. doi: 10.1016/j.ajhg.2009.07.017.
Am J Hum Genet. 2009.
PMID: 19732867
Free PMC article.
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Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
Schultz JM, Khan SN, Ahmed ZM, Riazuddin S, Waryah AM, Chhatre D, Starost MF, Ploplis B, Buckley S, Velásquez D, Kabra M, Lee K, Hassan MJ, Ali G, Ansar M, Ghosh M, Wilcox ER, Ahmad W, Merlino G, Leal SM, Riazuddin S, Friedman TB, Morell RJ.
Schultz JM, et al.
Am J Hum Genet. 2009 Jul;85(1):25-39. doi: 10.1016/j.ajhg.2009.06.003. Epub 2009 Jul 2.
Am J Hum Genet. 2009.
PMID: 19576567
Free PMC article.
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The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3.
Ain Q, Nazli S, Riazuddin S, Jaleel AU, Riazuddin SA, Zafar AU, Khan SN, Husnain T, Griffith AJ, Ahmed ZM, Friedman TB, Riazuddin S.
Ain Q, et al.
Hum Genet. 2007 Dec;122(5):445-50. doi: 10.1007/s00439-007-0418-z. Epub 2007 Aug 10.
Hum Genet. 2007.
PMID: 17690910
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A new locus for nonsyndromic deafness DFNB49 maps to chromosome 5q12.3-q14.1.
Ramzan K, Shaikh RS, Ahmad J, Khan SN, Riazuddin S, Ahmed ZM, Friedman TB, Wilcox ER, Riazuddin S.
Ramzan K, et al.
Hum Genet. 2005 Jan;116(1-2):17-22. doi: 10.1007/s00439-004-1205-8. Epub 2004 Nov 6.
Hum Genet. 2005.
PMID: 15538632
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