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WILLIAM NANCE, D.M.D.
D.M.D.
General Practice Dentistry
NPI: 1376578278Individual
Specialties, Licenses & Credentials
General Practice DentistryPrimary
Dentist — General Practice
Code: 1223G0001X
5046(KY)
Research & Publications (20)
Transient pretreatment with glucocorticoid ablates innate toxicity of systemically delivered adenoviral vectors without reducing efficacy.
PMID 19174760·Mol Ther·2009
7-preclinical
Segregation of enlarged vestibular aqueducts in families with non-diagnostic SLC26A4 genotypes.
PMID 19578036·J Med Genet·2009
8-other
Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?
PMID 19204907·Hum Mutat·2009
7-preclinical
Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNA(Ser(UCN)) in sensorineural hearing loss.
PMID 18028453·Clin Genet·2008
8-other
Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia.
PMID 18435799·Clin Genet·2008
8-other
A comparative analysis of the genetic epidemiology of deafness in the United States in two sets of pedigrees collected more than a century apart.
PMID 18656178·Am J Hum Genet·2008
4-observational
Studies of age-correlated features of cognitive-behavioral development in children and adolescents with genetic disorders.
PMID 17853466·Am J Med Genet A·2007
4-observational
Familial unilateral deafness and delayed endolymphatic hydrops.
PMID 17497713·Am J Med Genet A·2007
5-case
Does universal newborn hearing screening identify all children with GJB2 (Connexin 26) deafness? Penetrance of GJB2 deafness.
PMID 17086082·Ear Hear·2006
5-case
Importance of congenital cytomegalovirus infections as a cause for pre-lingual hearing loss.
PMID 16384744·J Clin Virol·2006
8-other
A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12.
PMID 15958501·J Med Genet·2006
8-other
Education in the genetics of hearing loss: a survey of early hearing detection and intervention programs.
PMID 16912582·Genet Med·2006
8-other
SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities.
PMID 15689455·J Med Genet·2005
8-other
A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment.
PMID 15994881·J Med Genet·2005
4-observational
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population.
PMID 15660226·Hum Genet·2005
8-other
Superficial siderosis: a potentially important cause of genetic as well as non-genetic deafness.
PMID 15368490·Am J Med Genet A·2004
5-case
Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study.
PMID 14571368·Am J Hum Genet·2003
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 501 MAIN STREET
HAWESVILLE, KY 42348 - Phone
- (270) 927-6653
Quick Facts
- NPI
- 1376578278
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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