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Page 1
Familial large vestibular aqueduct syndrome.
Griffith AJ, Arts A, Downs C, Innis JW, Shepard NT, Sheldon S, Gebarski SS. Griffith AJ, et al. Laryngoscope. 1996 Aug;106(8):960-5. doi: 10.1097/00005537-199608000-00009. Laryngoscope. 1996. PMID: 8699909
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
Clinical manifestations of DFNB29 deafness.
Ahmed ZM, Riazuddin S, Friedman TB, Riazuddin S, Wilcox ER, Griffith AJ. Ahmed ZM, et al. Among authors: griffith aj. Adv Otorhinolaryngol. 2002;61:156-60. doi: 10.1159/000066828. Adv Otorhinolaryngol. 2002. PMID: 12408079 No abstract available.
The Stickler syndrome: genotype/phenotype correlation in 10 families with Stickler syndrome resulting from seven mutations in the type II collagen gene locus COL2A1.
Liberfarb RM, Levy HP, Rose PS, Wilkin DJ, Davis J, Balog JZ, Griffith AJ, Szymko-Bennett YM, Johnston JJ, Francomano CA, Tsilou E, Rubin BI. Liberfarb RM, et al. Among authors: griffith aj. Genet Med. 2003 Jan-Feb;5(1):21-7. doi: 10.1097/00125817-200301000-00004. Genet Med. 2003. PMID: 12544472 Free article. Review.
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.
Stickler syndrome: clinical characteristics and diagnostic criteria.
Rose PS, Levy HP, Liberfarb RM, Davis J, Szymko-Bennett Y, Rubin BI, Tsilou E, Griffith AJ, Francomano CA. Rose PS, et al. Among authors: griffith aj. Am J Med Genet A. 2005 Oct 15;138A(3):199-207. doi: 10.1002/ajmg.a.30955. Am J Med Genet A. 2005. PMID: 16152640
158 results