Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
3R01DC002530-02S1
Application #
2767120
Study Section
Mammalian Genetics Study Section (MGN)
Project Start
1997-07-01
Project End
2002-06-30
Budget Start
1998-07-01
Budget End
1999-06-30
Support Year
2
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Virginia Commonwealth University
Department
Genetics
Type
Schools of Medicine
DUNS #
City
Richmond
State
VA
Country
United States
Zip Code
23298
Tekin, Mustafa; Xia, Xia-Juan; Erdenetungalag, Radnaabazar et al. (2010) GJB2 mutations in Mongolia: complex alleles, low frequency, and reduced fitness of the deaf. Ann Hum Genet 74:155-64
Nance, Walter E (2003) The genetics of deafness. Ment Retard Dev Disabil Res Rev 9:109-19
Park, H-J; Shaukat, S; Liu, X-Z et al. (2003) Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness. J Med Genet 40:242-8
Stern, S J; Arnos, K S; Murrelle, L et al. (2002) Attitudes of deaf and hard of hearing subjects towards genetic testing and prenatal diagnosis of hearing loss. J Med Genet 39:449-53
Liu, Xue Zhong; Xia, Xia Juan; Ke, Xiao Mei et al. (2002) The prevalence of connexin 26 ( GJB2) mutations in the Chinese population. Hum Genet 111:394-7
Zwaenepoel, I; Verpy, E; Blanchard, S et al. (2001) Identification of three novel mutations in the USH1C gene and detection of thirty-one polymorphisms used for haplotype analysis. Hum Mutat 17:34-41
Liu, X Z; Xu, L R; Hu, Y et al. (2001) Epidemiological studies on hearing impairment with reference to genetic factors in Sichuan, China. Ann Otol Rhinol Laryngol 110:356-63
Bork, J M; Peters, L M; Riazuddin, S et al. (2001) Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23. Am J Hum Genet 68:26-37
Tekin, M; Akar, N; Cin, S et al. (2001) Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians. Hum Genet 108:385-9
Tekin, M; Arnos, K S; Xia, X J et al. (2001) W44C mutation in the connexin 26 gene associated with dominant non-syndromic deafness. Clin Genet 59:269-73

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