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Page 1
Auditory dysfunction in Stickler syndrome.
Szymko-Bennett YM, Mastroianni MA, Shotland LI, Davis J, Ondrey FG, Balog JZ, Rudy SF, McCullagh L, Levy HP, Liberfarb RM, Francomano CA, Griffith AJ. Szymko-Bennett YM, et al. Among authors: griffith aj. Arch Otolaryngol Head Neck Surg. 2001 Sep;127(9):1061-8. doi: 10.1001/archotol.127.9.1061. Arch Otolaryngol Head Neck Surg. 2001. PMID: 11556853
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
Kurima K, Peters LM, Yang Y, Riazuddin S, Ahmed ZM, Naz S, Arnaud D, Drury S, Mo J, Makishima T, Ghosh M, Menon PS, Deshmukh D, Oddoux C, Ostrer H, Khan S, Riazuddin S, Deininger PL, Hampton LL, Sullivan SL, Battey JF Jr, Keats BJ, Wilcox ER, Friedman TB, Griffith AJ. Kurima K, et al. Among authors: griffith aj. Nat Genet. 2002 Mar;30(3):277-84. doi: 10.1038/ng842. Epub 2002 Feb 19. Nat Genet. 2002. PMID: 11850618
A mutation of PCDH15 among Ashkenazi Jews with the type 1 Usher syndrome.
Ben-Yosef T, Ness SL, Madeo AC, Bar-Lev A, Wolfman JH, Ahmed ZM, Desnick RJ, Willner JP, Avraham KB, Ostrer H, Oddoux C, Griffith AJ, Friedman TB. Ben-Yosef T, et al. Among authors: griffith aj. N Engl J Med. 2003 Apr 24;348(17):1664-70. doi: 10.1056/NEJMoa021502. N Engl J Med. 2003. PMID: 12711741 Free article. No abstract available.
Recent advances in the understanding of syndromic forms of hearing loss.
Friedman TB, Schultz JM, Ben-Yosef T, Pryor SP, Lagziel A, Fisher RA, Wilcox ER, Riazuddin S, Ahmed ZM, Belyantseva IA, Griffith AJ. Friedman TB, et al. Among authors: griffith aj. Ear Hear. 2003 Aug;24(4):289-302. doi: 10.1097/01.AUD.0000079804.00047.CE. Ear Hear. 2003. PMID: 12923420 Review. No abstract available.
Human nonsyndromic sensorineural deafness.
Friedman TB, Griffith AJ. Friedman TB, et al. Among authors: griffith aj. Annu Rev Genomics Hum Genet. 2003;4:341-402. doi: 10.1146/annurev.genom.4.070802.110347. Annu Rev Genomics Hum Genet. 2003. PMID: 14527306 Review.
160 results