Pandya A - Search Results

1

Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity.

Pandya A, Xia X, Radnaabazar J, Batsuuri J, Dangaansuren B, Fischel-Ghodsian N, Nance WE. Pandya A, et al. J Med Genet. 1997 Feb;34(2):169-72. doi: 10.1136/jmg.34.2.169. J Med Genet. 1997. PMID: 9039999 Free PMC article.

2

Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands.

Pandya A, Arnos KS, Xia XJ, Welch KO, Blanton SH, Friedman TB, Garcia Sanchez G, Liu MD XZ, Morell R, Nance WE. Pandya A, et al. Genet Med. 2003 Jul-Aug;5(4):295-303. doi: 10.1097/01.GIM.0000078026.01140.68. Genet Med. 2003. PMID: 12865758

3

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: pandya a. Hum Mol Genet. 2000 Jan 1;9(1):63-7. doi: 10.1093/hmg/9.1.63. Hum Mol Genet. 2000. PMID: 10587579

4

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: pandya a. Clin Genet. 2001 Apr;59(4):269-73. doi: 10.1034/j.1399-0004.2001.590409.x. Clin Genet. 2001. PMID: 11298683

5

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: pandya a. Hum Genet. 2001 May;108(5):385-9. doi: 10.1007/s004390100507. Hum Genet. 2001. PMID: 11409864

6

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: pandya a. Hum Mol Genet. 2001 Dec 1;10(25):2945-51. doi: 10.1093/hmg/10.25.2945. Hum Mol Genet. 2001. PMID: 11741837

7

GJB2 mutations in Mongolia: complex alleles, low frequency, and reduced fitness of the deaf.

Tekin M, Xia XJ, Erdenetungalag R, Cengiz FB, White TW, Radnaabazar J, Dangaasuren B, Tastan H, Nance WE, Pandya A. Tekin M, et al. Among authors: pandya a. Ann Hum Genet. 2010 Mar;74(2):155-64. doi: 10.1111/j.1469-1809.2010.00564.x. Epub 2010 Jan 27. Ann Hum Genet. 2010. PMID: 20201936 Free PMC article.

8

Vestibular dysfunction in DFNB1 deafness.

Dodson KM, Blanton SH, Welch KO, Norris VW, Nuzzo RL, Wegelin JA, Marin RS, Nance WE, Pandya A, Arnos KS. Dodson KM, et al. Among authors: pandya a. Am J Med Genet A. 2011 May;155A(5):993-1000. doi: 10.1002/ajmg.a.33828. Epub 2011 Apr 4. Am J Med Genet A. 2011. PMID: 21465647 Free PMC article.

9

The clinical and audiologic features of hearing loss due to mitochondrial mutations.

Yelverton JC, Arnos K, Xia XJ, Nance WE, Pandya A, Dodson KM. Yelverton JC, et al. Among authors: pandya a. Otolaryngol Head Neck Surg. 2013 Jun;148(6):1017-22. doi: 10.1177/0194599813482705. Epub 2013 Mar 22. Otolaryngol Head Neck Surg. 2013. PMID: 23525847

10

Implications of molecular diagnostic testing in families with hereditary pancreatitis.

Pandya A, Xia XJ, Blanton SH, Landa B, Markello T, Nance WE. Pandya A, et al. Genet Test. 1997-1998;1(3):207-11. doi: 10.1089/gte.1997.1.207. Genet Test. 1997. PMID: 10464647

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

856 results

Search Page

Filters