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Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|December 3, 2009
[Analysis of the parental origin of de novo MECP2 mutations and X chromosome inactivation in fifteen sporadic cases with Rett syndrome]Xing-wang Zhu, Hong Pan, Mei-rong Li, et al.Toxicology Letters|February 20, 2010
Dynamic pattern of gene expression of ZnT-1, ZnT-3 and PRG-1 in rat brain following flurothyl-induced recurrent neonatal seizuresHong Ni, Yu-wu Jiang, Zhuo-jun Xiao, et al.Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|June 20, 2006
[MECP2 gene mutations in twenty-six cases with atypical Rett syndrome]Mei-rong Li, Hong Pan, Xin-hua Bao, et al.Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|January 16, 2007
[X chromosome inactivation patterns in patients with Rett syndrome and their mothers and the parental origin of the priority inactive X chromosome]Sheng-ling Jiang, Xin-hua Bao, Fu-ying Song, et al.European Journal of Human Genetics : EJHG|July 12, 2002
MECP2 gene mutation analysis in Chinese patients with Rett syndromeHong Pan, Yan-Ping Wang, Xing-Hua Bao, et al.Pediatric Neurology|August 10, 2005
ABCD1 gene mutations in Chinese patients with X-linked adrenoleukodystrophyHong Pan, Hui Xiong, Ye Wu, et al.Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|November 20, 2012
[Phenotype and SCN1A gene mutation screening in 39 families with generalized epilepsy with febrile seizures plus]Xiao-jing Xu, Yue-hua Zhang, Hui-hui Sun, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 11, 2012
[Genetic and phenotypic characteristics of SCN1A mutations in Dravet syndrome]Xiao-jing Xu, Yue-hua Zhang, Hui-hui Sun, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 10, 2004
[X-linked adrenoleukodystrophy ABCD1 gene mutation analysis in China]Hong Pan, Hui Xiong, Yue-hua Zhang, et al.Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|February 6, 2004
[Clinical characteristics of X-linked adrenoleukodystrophy]Hui Xiong, Yue-hua Zhang, Jiong Qin, et al.Pageof 8