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Acta Oto-Laryngologica|December 5, 2015
The role of transcription factors of neurosensory cells in non-syndromic sensorineural hearing loss with or without inner ear malformationYuan Zhou, Jie Qing, Yunpeng Dong, et al.Kidney & Blood Pressure Research|February 28, 2019
Paternal Programming of Liver Function and Lipid Profile Induced by a Paternal Pre-Conceptional Unhealthy Diet: Potential Association with Altered Gut Microbiome CompositionXiaoli Zhang, Yunpeng Dong, Guoying Sun, et al.Anatomical Record (Hoboken, N.J. : 2007)|December 27, 2019
Congenital Middle Ear Malformation with Common Deafness Gene Mutation Analysis: A Review of 813 Profound Sensorineural Hearing Loss Child PatientsYunpeng Dong, Xiangbo He, Weijing Wu, et al.Pharmacogenomics and Personalized Medicine|September 9, 2020
The Relationship Between Single Nucleotide Polymorphisms of SMAD3/SMAD6 and Risk of Esophageal Squamous Cell Carcinoma in Chinese PopulationJinjie Yu, Yunpeng Dong, Weifeng Tang, et al.Plos One|May 26, 2017
A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese familyZhijie Niu, Yong Feng, Lingyun Mei, et al.Pageof 3