Your search returned 17 results.

Results
	1.	[Giant cell reparative granuloma of the temporal bone: A case report]. [electronic resource] by Song, Jian Mei, Lingyun Cai, Xinzhang Producer: 20191017 In: Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	[The application of 3D reconstruction of CT scans for the observation of the cochlear implanted electrode location]. [electronic resource] by Liu, Hanbo Feng, Yong Chen, Dengming CaI, Xinzhang He, Chufeng Producer: 20110407 In: Lin chuang er bi yan hou ke za zhi = Journal of clinical otorhinolaryngology vol. 20 Availability: No items available. Save to lists Add to cart (remove)
	3.	[Study of the anatomy related to cochlear implantation guided by HRCT]. [electronic resource] by He, Xuebin Feng, Yong Chen, Dengming Mei, Lingyun He, Chufeng Cai, Xinzhang Producer: 20111128 In: Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery vol. 25 Availability: No items available. Save to lists Add to cart (remove)
	4.	[Inhibition of the expression of VEGF gene in nasopharyngeal carcinoma cells by microRNA]. [electronic resource] by Cai, Xinzhang Wei, Wei Zhao, Suping Tang, Yaoyun He, Chufeng Wang, Chenglong Producer: 20110825 In: Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	5.	[Surgical approaches and related microsurgical anatomy about suprameatal approach: new surgical approach for cochlear implantation]. [electronic resource] by Liu, Hanbo Feng, Yong Chen, Dengming Mei, Lingyun He, Chufeng Cai, Xinzhang Producer: 20110602 In: Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery vol. 21 Availability: No items available. Save to lists Add to cart (remove)
	6.	Novel missense mutation in the COL3A1 gene caused vascular Ehlers-Danlos syndrome in a Chinese family. [electronic resource] by He, Fang Wang, Xianwei Cai, Xinzhang Peng, Hao Zhang, Lusi Zhu, Tengfei Xia, Kun Pan, Qian Hu, Zhengmao Producer: 20161014 In: The Journal of dermatology vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing. [electronic resource] by Li, Wu Mei, Lingyun Chen, Hongsheng Cai, Xinzhang Liu, Yalan Men, Meichao Liu, Xue Zhong Yan, Denise Ling, Jie Feng, Yong Producer: 20190513 In: Neural plasticity vol. 2019 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	A New Genetic Diagnostic for Enlarged Vestibular Aqueduct Based on Next-Generation Sequencing. [electronic resource] by Liu, Yalan Wang, Lili Feng, Yong He, Chufeng Liu, Deyuan Cai, Xinzhang Jiang, Lu Chen, Hongsheng Liu, Chang Wu, Hong Mei, Lingyun Producer: 20170630 In: PloS one vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Downregulation of p66Shc can reduce oxidative stress and apoptosis in oxidative stress model of marginal cells of stria vascularis in Sprague Dawley rats. [electronic resource] by Hao, Cong Wu, Xuewen Zhou, Ruoyu Zhang, Hao Zhou, Yulai Wang, Xinxing Feng, Yong Mei, Lingyun He, Chufeng Cai, Xinzhang Wu, Lisha Producer: 20200423 In: Drug design, development and therapy vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Identification and functional analysis of a novel mutation in the PAX3 gene associated with Waardenburg syndrome type I. [electronic resource] by Niu, Zhijie Li, Jiada Tang, Fen Sun, Jie Wang, Xueping Jiang, Lu Mei, Lingyun Chen, Hongsheng Liu, Yalan Cai, Xinzhang Feng, Yong He, Chufeng Producer: 20171226 In: Gene vol. 642 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family. [electronic resource] by Niu, Zhijie Feng, Yong Mei, Lingyun Sun, Jie Wang, Xueping Wang, Juncheng Hu, Zhengmao Dong, Yunpeng Chen, Hongsheng He, Chufeng Liu, Yalan Cai, Xinzhang Liu, Xuezhong Jiang, Lu Producer: 20170911 In: PloS one vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Reproductive guidance through prenatal diagnosis and genetic counseling for recessive hereditary hearing loss in high-risk families. [electronic resource] by Deng, Yuyuan Sang, Shushan Wen, Jie Liu, Yalan Ling, Jie Chen, Hongsheng Cai, Xinzhang Mei, Lingyun Chen, Xiaoya Li, Meng Li, Wu Li, Taoxi He, Chufeng Feng, Yong Producer: 20190111 In: International journal of pediatric otorhinolaryngology vol. 115 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Proband Whole-Exome Sequencing Identified Genes Responsible for Autosomal Recessive Non-Syndromic Hearing Loss in 33 Chinese Nuclear Families. [electronic resource] by Sang, Shushan Ling, Jie Liu, Xuezhong Mei, Lingyun Cai, Xinzhang Li, Taoxi Li, Wu Li, Meng Wen, Jie Liu, Xianlin Liu, Jing Liu, Yalan Chen, Hongsheng He, Chufeng Feng, Yong Publication details: Frontiers in genetics 2019 In: Frontiers in genetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Exome sequencing identifies a novel missense mutation of WFS1 as the cause of non-syndromic low-frequency hearing loss in a Chinese family. [electronic resource] by Niu, Zhijie Feng, Yong Hu, Zhengmao Li, Jiada Sun, Jie Chen, Hongsheng He, Chufeng Wang, Xueping Jiang, Lu Liu, Yalan Cai, Xinzhang Wang, Lili Cai, Yuxiang Liu, Xuezhong Mei, Lingyun Producer: 20171002 In: International journal of pediatric otorhinolaryngology vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	A novel mutation in the SMPX gene associated with X-linked nonsyndromic sensorineural hearing loss in a Chinese family. [electronic resource] by Deng, Yuyuan Niu, Zhijie Fan, LiangLiang Ling, Jie Chen, Hongsheng Cai, Xinzhang Mei, Lingyun He, Chufeng Zhang, Xuewei Wen, Jie Li, Meng Li, Wu Li, Taoxi Sang, Shushan Liu, Yalan Feng, Yong Producer: 20180924 In: Journal of human genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	New ZNF644 mutations identified in patients with high myopia. [electronic resource] by Xiang, Xinying Wang, Tianyun Tong, Ping Li, Yunping Guo, Hui Wan, Anran Xia, Lu Liu, Yanling Li, Ying Tian, Qi Shen, Lu Cai, Xinzhang Tian, Lei Jin, Xuemin Xia, Kun Hu, Zhengmao Producer: 20140930 In: Molecular vision vol. 20 Availability: No items available. Save to lists Add to cart (remove)
	17.	Extrusion pump ABCC1 was first linked with nonsyndromic hearing loss in humans by stepwise genetic analysis. [electronic resource] by Li, Meng Mei, Lingyun He, Chufeng Chen, Hongsheng Cai, Xinzhang Liu, Yalan Tian, Runyi Tian, Qi Song, Jian Jiang, Lu Liu, Chang Wu, Hong Li, Taoxi Liu, Jing Li, Ximan Yi, Yifang Yan, Denise Blanton, Susan H Hu, Zhengmao Liu, Xuezhong Li, Jiada Ling, Jie Feng, Yong Producer: 20200501 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)