Griffith AJ - Search Results

1

SLC26A4-linked CEVA haplotype correlates with phenotype in patients with enlargement of the vestibular aqueduct.

Chao JR, Chattaraj P, Munjal T, Honda K, King KA, Zalewski CK, Chien WW, Brewer CC, Griffith AJ. Chao JR, et al. Among authors: griffith aj. BMC Med Genet. 2019 Jul 2;20(1):118. doi: 10.1186/s12881-019-0853-4. BMC Med Genet. 2019. PMID: 31266487 Free PMC article.

2

Audiovestibular phenotype associated with a COL11A1 mutation in Marshall syndrome.

Griffith AJ, Gebarski SS, Shepard NT, Kileny PR. Griffith AJ, et al. Arch Otolaryngol Head Neck Surg. 2000 Jul;126(7):891-4. doi: 10.1001/archotol.126.7.891. Arch Otolaryngol Head Neck Surg. 2000. PMID: 10889003

3

Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delT.

Griffith AJ, Chowdhry AA, Kurima K, Hood LJ, Keats B, Berlin CI, Morell RJ, Friedman TB. Griffith AJ, et al. Am J Hum Genet. 2000 Sep;67(3):745-9. doi: 10.1086/303045. Epub 2000 Jul 19. Am J Hum Genet. 2000. PMID: 10903123 Free PMC article.

4

Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness.

Park HJ, Shaukat S, Liu XZ, Hahn SH, Naz S, Ghosh M, Kim HN, Moon SK, Abe S, Tukamoto K, Riazuddin S, Kabra M, Erdenetungalag R, Radnaabazar J, Khan S, Pandya A, Usami SI, Nance WE, Wilcox ER, Riazuddin S, Griffith AJ. Park HJ, et al. Among authors: griffith aj. J Med Genet. 2003 Apr;40(4):242-8. doi: 10.1136/jmg.40.4.242. J Med Genet. 2003. PMID: 12676893 Free PMC article.

5

Genetic homogeneity and phenotypic variability among Ashkenazi Jews with Usher syndrome type III.

Ness SL, Ben-Yosef T, Bar-Lev A, Madeo AC, Brewer CC, Avraham KB, Kornreich R, Desnick RJ, Willner JP, Friedman TB, Griffith AJ. Ness SL, et al. Among authors: griffith aj. J Med Genet. 2003 Oct;40(10):767-72. doi: 10.1136/jmg.40.10.767. J Med Genet. 2003. PMID: 14569126 Free PMC article. No abstract available.

6

Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction.

Naz S, Griffith AJ, Riazuddin S, Hampton LL, Battey JF Jr, Khan SN, Riazuddin S, Wilcox ER, Friedman TB. Naz S, et al. Among authors: griffith aj. J Med Genet. 2004 Aug;41(8):591-5. doi: 10.1136/jmg.2004.018523. J Med Genet. 2004. PMID: 15286153 Free PMC article.

7

Early onset and rapid progression of dominant nonsyndromic DFNA36 hearing loss.

Makishima T, Kurima K, Brewer CC, Griffith AJ. Makishima T, et al. Among authors: griffith aj. Otol Neurotol. 2004 Sep;25(5):714-9. doi: 10.1097/00129492-200409000-00011. Otol Neurotol. 2004. PMID: 15354000

8

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.

Pryor SP, Madeo AC, Reynolds JC, Sarlis NJ, Arnos KS, Nance WE, Yang Y, Zalewski CK, Brewer CC, Butman JA, Griffith AJ. Pryor SP, et al. Among authors: griffith aj. J Med Genet. 2005 Feb;42(2):159-65. doi: 10.1136/jmg.2004.024208. J Med Genet. 2005. PMID: 15689455 Free PMC article. No abstract available.

9

Investigation of the role of congenital cytomegalovirus infection in the etiology of enlarged vestibular aqueducts.

Pryor SP, Demmler GJ, Madeo AC, Yang Y, Zalewski CK, Brewer CC, Butman JA, Fowler KB, Griffith AJ. Pryor SP, et al. Among authors: griffith aj. Arch Otolaryngol Head Neck Surg. 2005 May;131(5):388-92. doi: 10.1001/archotol.131.5.388. Arch Otolaryngol Head Neck Surg. 2005. PMID: 15897416

10

Multiple quantitative trait loci modify cochlear hair cell degeneration in the Beethoven (Tmc1Bth) mouse model of progressive hearing loss DFNA36.

Noguchi Y, Kurima K, Makishima T, de Angelis MH, Fuchs H, Frolenkov G, Kitamura K, Griffith AJ. Noguchi Y, et al. Among authors: griffith aj. Genetics. 2006 Aug;173(4):2111-9. doi: 10.1534/genetics.106.057372. Epub 2006 Apr 28. Genetics. 2006. PMID: 16648588 Free PMC article.

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