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Deafness gene mutations in newborns in Beijing.
Han S, Yang X, Zhou Y, Hao J, Shen A, Xu F, Chu P, Jin Y, Lu J, Guo Y, Shi J, Liu H, Ni X. Han S, et al. Among authors: hao j. Acta Otolaryngol. 2016;136(5):475-9. doi: 10.3109/00016489.2015.1128121. Epub 2016 Jan 14. Acta Otolaryngol. 2016. PMID: 26766211
Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China.
Dai P, Huang LH, Wang GJ, Gao X, Qu CY, Chen XW, Ma FR, Zhang J, Xing WL, Xi SY, Ma BR, Pan Y, Cheng XH, Duan H, Yuan YY, Zhao LP, Chang L, Gao RZ, Liu HH, Zhang W, Huang SS, Kang DY, Liang W, Zhang K, Jiang H, Guo YL, Zhou Y, Zhang WX, Lyu F, Jin YN, Zhou Z, Lu HL, Zhang X, Liu P, Ke J, Hao JS, Huang HM, Jiang D, Ni X, Long M, Zhang L, Qiao J, Morton CC, Liu XZ, Cheng J, Han DM. Dai P, et al. Among authors: hao js. Am J Hum Genet. 2019 Oct 3;105(4):803-812. doi: 10.1016/j.ajhg.2019.09.003. Epub 2019 Sep 26. Am J Hum Genet. 2019. PMID: 31564438 Free PMC article.
The treatment for the first branchial cleft anomalies in children.
Liu W, Chen M, Hao J, Yang Y, Zhang J, Ni X. Liu W, et al. Among authors: hao j. Eur Arch Otorhinolaryngol. 2017 Sep;274(9):3465-3470. doi: 10.1007/s00405-017-4648-y. Epub 2017 Jun 20. Eur Arch Otorhinolaryngol. 2017. PMID: 28634783
6,780 results