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An autosomal genomic scan for loci linked to type 2 diabetes in northern Han Chinese.
Zhao JY, Xiong MM, Huang W, Wang H, Zuo J, Wu GD, Chen Z, Qiang BQ, Zhang ML, Chen JL, Ding W, Yuan WT, Xu HY, Jin L, Li YX, Sun Q, Liu QY, Boerwinkle E, Fang FD. Zhao JY, et al. Among authors: sun q. J Mol Med (Berl). 2005 Mar;83(3):209-15. doi: 10.1007/s00109-004-0587-3. Epub 2004 Nov 11. J Mol Med (Berl). 2005. PMID: 15776287
A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family.
Cheng J, Han DY, Dai P, Sun HJ, Tao R, Sun Q, Yan D, Qin W, Wang HY, Ouyang XM, Yang SZ, Cao JY, Feng GY, Du LL, Zhang YZ, Zhai SQ, Yang WY, Liu XZ, He L, Yuan HJ. Cheng J, et al. Among authors: sun hj, sun q. Clin Genet. 2007 Nov;72(5):471-7. doi: 10.1111/j.1399-0004.2007.00889.x. Epub 2007 Sep 14. Clin Genet. 2007. PMID: 17868390
Toxic epidermal necrolysis complicated by Mucor infection.
Jin H, Qiao J, Wang B, Wang H, Sun Q. Jin H, et al. Among authors: sun q. Int J Dermatol. 2008 Apr;47(4):383-6. doi: 10.1111/j.1365-4632.2008.03421.x. Int J Dermatol. 2008. PMID: 18377605 No abstract available.
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