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Page 1
GJB2 mutation spectrum in 2,063 Chinese patients with nonsyndromic hearing impairment.
Dai P, Yu F, Han B, Liu X, Wang G, Li Q, Yuan Y, Liu X, Huang D, Kang D, Zhang X, Yuan H, Yao K, Hao J, He J, He Y, Wang Y, Ye Q, Yu Y, Lin H, Liu L, Deng W, Zhu X, You Y, Cui J, Hou N, Xu X, Zhang J, Tang L, Song R, Lin Y, Sun S, Zhang R, Wu H, Ma Y, Zhu S, Wu BL, Han D, Wong LJ. Dai P, et al. Among authors: wu h, wu bl. J Transl Med. 2009 Apr 14;7:26. doi: 10.1186/1479-5876-7-26. J Transl Med. 2009. PMID: 19366456 Free PMC article.
Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss.
Dai P, Stewart AK, Chebib F, Hsu A, Rozenfeld J, Huang D, Kang D, Lip V, Fang H, Shao H, Liu X, Yu F, Yuan H, Kenna M, Miller DT, Shen Y, Yang W, Zelikovic I, Platt OS, Han D, Alper SL, Wu BL. Dai P, et al. Among authors: wu bl. Physiol Genomics. 2009 Aug 7;38(3):281-90. doi: 10.1152/physiolgenomics.00047.2009. Epub 2009 Jun 9. Physiol Genomics. 2009. PMID: 19509082
Audiologic phenotype and progression in GJB2 (Connexin 26) hearing loss.
Kenna MA, Feldman HA, Neault MW, Frangulov A, Wu BL, Fligor B, Rehm HL. Kenna MA, et al. Among authors: wu bl. Arch Otolaryngol Head Neck Surg. 2010 Jan;136(1):81-7. doi: 10.1001/archoto.2009.202. Arch Otolaryngol Head Neck Surg. 2010. PMID: 20083784 Free PMC article.
A map of copy number variations in Chinese populations.
Lou H, Li S, Yang Y, Kang L, Zhang X, Jin W, Wu B, Jin L, Xu S. Lou H, et al. PLoS One. 2011;6(11):e27341. doi: 10.1371/journal.pone.0027341. Epub 2011 Nov 7. PLoS One. 2011. PMID: 22087296 Free PMC article.
238 results