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Newborn hearing concurrent genetic screening for hearing impairment-a clinical practice in 58,397 neonates in Tianjin, China.
Zhang J, Wang P, Han B, Ding Y, Pan L, Zou J, Liu H, Pang X, Liu E, Wang H, Liu H, Zhang X, Cheng X, Feng D, Li Q, Wang D, Zong L, Yi Y, Tian N, Mu F, Tian G, Chen Y, Liu G, Zhang F, Yi X, Yang L, Wang Q. Zhang J, et al. Among authors: yi x, yi y. Int J Pediatr Otorhinolaryngol. 2013 Dec;77(12):1929-35. doi: 10.1016/j.ijporl.2013.08.038. Epub 2013 Sep 8. Int J Pediatr Otorhinolaryngol. 2013. PMID: 24100002
Targeted high-throughput sequencing identifies pathogenic mutations in KCNQ4 in two large Chinese families with autosomal dominant hearing loss.
Wang H, Zhao Y, Yi Y, Gao Y, Liu Q, Wang D, Li Q, Lan L, Li N, Guan J, Yin Z, Han B, Zhao F, Zong L, Xiong W, Yu L, Song L, Yi X, Yang L, Petit C, Wang Q. Wang H, et al. Among authors: yi x, yi y. PLoS One. 2014 Aug 12;9(8):e103133. doi: 10.1371/journal.pone.0103133. eCollection 2014. PLoS One. 2014. PMID: 25116015 Free PMC article.
Comprehensive carrier genetic test using next-generation deoxyribonucleic acid sequencing in infertile couples wishing to conceive through assisted reproductive technology.
Martin J, Asan, Yi Y, Alberola T, Rodríguez-Iglesias B, Jiménez-Almazán J, Li Q, Du H, Alama P, Ruiz A, Bosch E, Garrido N, Simon C. Martin J, et al. Among authors: yi y. Fertil Steril. 2015 Nov;104(5):1286-93. doi: 10.1016/j.fertnstert.2015.07.1166. Epub 2015 Sep 3. Fertil Steril. 2015. PMID: 26354092 Free article.
Carney complex with PRKAR1A gene mutation: A case report and literature review.
Liu Q, Tong D, Liu G, Yi Y, Zhang D, Zhang J, Zhang Y, Huang Z, Li Y, Chen R, Guan Y, Yi X, Jiang J. Liu Q, et al. Among authors: yi x, yi y. Medicine (Baltimore). 2017 Dec;96(50):e8999. doi: 10.1097/MD.0000000000008999. Medicine (Baltimore). 2017. PMID: 29390296 Free PMC article. Review.
4,694 results