Nance WE - Search Results

1

Epidemiological studies on hearing impairment with reference to genetic factors in Sichuan, China.

Liu XZ, Xu LR, Hu Y, Nance WE, Sismanis A, Zhang SL, Xu Y. Liu XZ, et al. Among authors: nance we. Ann Otol Rhinol Laryngol. 2001 Apr;110(4):356-63. doi: 10.1177/000348940111000412. Ann Otol Rhinol Laryngol. 2001. PMID: 11307913

2

Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss.

Liu XZ, Xia XJ, Xu LR, Pandya A, Liang CY, Blanton SH, Brown SD, Steel KP, Nance WE. Liu XZ, et al. Among authors: nance we. Hum Mol Genet. 2000 Jan 1;9(1):63-7. doi: 10.1093/hmg/9.1.63. Hum Mol Genet. 2000. PMID: 10587579

3

Superficial siderosis: a potentially important cause of genetic as well as non-genetic deafness.

Dodson KM, Sismanis A, Nance WE. Dodson KM, et al. Among authors: nance we. Am J Med Genet A. 2004 Sep 15;130A(1):22-5. doi: 10.1002/ajmg.a.30050. Am J Med Genet A. 2004. PMID: 15368490

4

Familial unilateral deafness and delayed endolymphatic hydrops.

Dodson KM, Kamei T, Sismanis A, Nance WE. Dodson KM, et al. Among authors: nance we. Am J Med Genet A. 2007 Jul 15;143A(14):1661-5. doi: 10.1002/ajmg.a.31741. Am J Med Genet A. 2007. PMID: 17497713

5

Relation between choice of partner and high frequency of connexin-26 deafness.

Nance WE, Liu XZ, Pandya A. Nance WE, et al. Lancet. 2000 Aug 5;356(9228):500-1. doi: 10.1016/S0140-6736(00)02565-4. Lancet. 2000. PMID: 10981905

6

Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians.

Tekin M, Akar N, Cin S, Blanton SH, Xia XJ, Liu XZ, Nance WE, Pandya A. Tekin M, et al. Among authors: nance we. Hum Genet. 2001 May;108(5):385-9. doi: 10.1007/s004390100507. Hum Genet. 2001. PMID: 11409864

7

Etiology of unilateral hearing loss in a national hereditary deafness repository.

Dodson KM, Georgolios A, Barr N, Nguyen B, Sismanis A, Arnos KS, Norris VW, Chapman D, Nance WE, Pandya A. Dodson KM, et al. Among authors: nance we. Am J Otolaryngol. 2012 Sep-Oct;33(5):590-4. doi: 10.1016/j.amjoto.2012.03.005. Epub 2012 Apr 24. Am J Otolaryngol. 2012. PMID: 22534022

8

W44C mutation in the connexin 26 gene associated with dominant non-syndromic deafness.

Tekin M, Arnos KS, Xia XJ, Oelrich MK, Liu XZ, Nance WE, Pandya A. Tekin M, et al. Among authors: nance we. Clin Genet. 2001 Apr;59(4):269-73. doi: 10.1034/j.1399-0004.2001.590409.x. Clin Genet. 2001. PMID: 11298683

9

Haplotype analysis of the USH1D locus and genotype-phenotype correlations.

Liu XZ, Blanton SH, Bitner-Glindzicz M, Pandya A, Landa B, MacArdle B, Rajput K, Bellman S, Webb BT, Ping X, Smith RJ, Nance WE. Liu XZ, et al. Among authors: nance we. Clin Genet. 2001 Jul;60(1):58-62. doi: 10.1034/j.1399-0004.2001.600109.x. Clin Genet. 2001. PMID: 11531971

10

Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness.

Liu XZ, Xia XJ, Adams J, Chen ZY, Welch KO, Tekin M, Ouyang XM, Kristiansen A, Pandya A, Balkany T, Arnos KS, Nance WE. Liu XZ, et al. Among authors: nance we. Hum Mol Genet. 2001 Dec 1;10(25):2945-51. doi: 10.1093/hmg/10.25.2945. Hum Mol Genet. 2001. PMID: 11741837

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