HuGE Literature Finder
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| New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing. Neural plasticity 2019 2019 7143458. Li Wu, Mei Lingyun, Chen Hongsheng, Cai Xinzhang, Liu Yalan, Men Meichao, Liu Xue Zhong, Yan Denise, Ling Jie, Feng Yo |
| Molecular etiology and genotype-phenotype correlation of Chinese Han deaf patients with type I and type II Waardenburg Syndrome. Scientific reports 2016 Oct 6 35498. Sun Lianhua, Li Xiaohua, Shi Jun, Pang Xiuhong, Hu Yechen, Wang Xiaowen, Wu Hao, Yang T |
| [Mutation analysis of seven patients with Waardenburg syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2016 Jun 33 (3): 312-5. Hao Ziqi, Zhou Yongan, Li Pengli, Zhang Quanbin, Li Jiao, Wang Pengfei, Li Xiangshao, Feng Yo |
| Clinical and genetic investigation of families with type II Waardenburg syndrome. Molecular medicine reports 2016 Jan . Chen Yong, Yang Fuwei, Zheng Hexin, Zhou Jianda, Zhu Ganghua, Hu Peng, Wu Weiji |
Genome-wide association study of three-dimensional facial morphology identifies a variant in PAX3 associated with nasion position.
American journal of human genetics 2012 Mar 90 (3): 478-85. Paternoster Lavinia, Zhurov Alexei I, Toma Arshed M, Kemp John P, St Pourcain Beate, Timpson Nicholas J, McMahon George, McArdle Wendy, Ring Susan M, Smith George Davey, Richmond Stephen, Evans David |
| Screening for novel PAX3 polymorphisms and risks of spina bifida. Birth defects research. Part A, Clinical and molecular teratology 2007 Jan 79 (1): 45-9. Lu Wei, Zhu Huiping, Wen Shu, Laurent Cecile, Shaw Gary M, Lammer Edward J, Finnell Richard |
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