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Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|December 23, 2008
[Clinical features and SCN1A gene mutation analysis of severe myoclonic epilepsy of infancy]Yue-hua Zhang, Hui-hui Sun, Xiao-yan Liu, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|March 15, 2008
[Detection of subtelomeric rearrangements in patients with idiopathic mental retardation/developmental delay]Ye Wu, Yu-wu Jiang, Xiao-zhu Wang, et al.
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences|April 20, 2011
[Clinical characteristics of Huntington disease in two pedigrees and analysis of expanded CAG trinucleotide repeat]Guang-na Cao, Xin-hua Bao, Hong-mei Lu, et al.
Chinese Medical Journal|November 26, 2008
Proteolipid protein 1 gene mutation in nine patients with Pelizaeus-Merzbacher diseaseJing-Min Wang, Ye Wu, Hui-Fang Wang, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|August 14, 2012
[Clinical and genetic study of twelve Chinese patients with Alexander disease]Li-li Zang, Ye Wu, Jing-min Wang, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|November 21, 2007
[Clinical characteristics and treatment of Rasmussen syndrome in 16 children]Yue-hua Zhang, Li-hua Pu, Xiao-yan Liu, et al.
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences|January 18, 2006
The genotype and phenotype studies of 40 Chinese patients with X-linked adrenoleukodystrophy (X-ALD)Li-li Ping, Xin-hua Bao, Ai-hua Wang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 9, 2010
[Analysis of the parental origin of MECP2 mutations in patients with Rett syndrome]Jing-jing Zhang, Xin-hua Bao, Guang-na Cao, et al.
Brain & Development|September 27, 2005
Genotype and early development in Rett syndrome: the value of international dataHelen Leonard, Hannah Moore, Mary Carey, et al.
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