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Page 1
Linkage of otosclerosis to a third locus (OTSC3) on human chromosome 6p21.3-22.3.
Chen W, Campbell CA, Green GE, Van Den Bogaert K, Komodikis C, Manolidis LS, Aconomou E, Kyamides Y, Christodoulou K, Faghel C, Giguére CM, Alford RL, Manolidis S, Van Camp G, Smith RJ. Chen W, et al. Among authors: green ge. J Med Genet. 2002 Jul;39(7):473-7. doi: 10.1136/jmg.39.7.473. J Med Genet. 2002. PMID: 12114476 Free PMC article.
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13).
McGuirt WT, Prasad SD, Griffith AJ, Kunst HP, Green GE, Shpargel KB, Runge C, Huybrechts C, Mueller RF, Lynch E, King MC, Brunner HG, Cremers CW, Takanosu M, Li SW, Arita M, Mayne R, Prockop DJ, Van Camp G, Smith RJ. McGuirt WT, et al. Among authors: green ge. Nat Genet. 1999 Dec;23(4):413-9. doi: 10.1038/70516. Nat Genet. 1999. PMID: 10581026
The M34T allele variant of connexin 26.
Cucci RA, Prasad S, Kelley PM, Green GE, Storm K, Willocx S, Cohn ES, Van Camp G, Smith RJ. Cucci RA, et al. Among authors: green ge. Genet Test. 2000;4(4):335-44. doi: 10.1089/109065700750065063. Genet Test. 2000. PMID: 11216656
Temporal bone histopathology in connexin 26-related hearing loss.
Jun AI, McGuirt WT, Hinojosa R, Green GE, Fischel-Ghodsian N, Smith RJ. Jun AI, et al. Among authors: green ge. Laryngoscope. 2000 Feb;110(2 Pt 1):269-75. doi: 10.1097/00005537-200002010-00016. Laryngoscope. 2000. PMID: 10680928
Genetic testing to identify deaf newborns.
Green GE, Smith RJ, Bent JP, Cohn ES. Green GE, et al. JAMA. 2000 Sep 13;284(10):1245. doi: 10.1001/jama.284.10.1245. JAMA. 2000. PMID: 10979110 No abstract available.
174 results