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Zhonghua Yi Xue Za Zhi|January 23, 2009
[Methylation-specific multiplex ligation-dependent probe amplification in diagnosis of Prader-Willi syndrome and Angelman syndrome]Mei-rong Li, Xiao-zhu Wang, Xiao-yan Liu, et al.
Research in Autism Spectrum Disorders|December 19, 2013
InterRett, a model for international data collection in a rare genetic disorderSandra Louise, Sue Fyfe, Ami Bebbington, et al.
Chinese Medical Journal|October 23, 2004
Case-control study and transmission/disequilibrium tests of the genes encoding GABRA5 and GABRB3 in a Chinese population affected by childhood absence epilepsyJian-jun Lü, Yue-hua Zhang, Hong Pan, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|April 19, 2005
[T-type calcium channel gene-CACNA1H is a susceptibility gene to childhood absence epilepsy]Jian-jun Lü, Yue-hua Zhang, Yu-cai Chen, et al.
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences|December 21, 2010
[Genotype, phenotype analysis and follow-up study on patients with Duchenne/Becker muscular dystrophy]Yan-zhi Zhang, Hui Xiong, Xiao-zhu Wang, et al.
Zhonghua Yi Xue Za Zhi|August 19, 2003
[Association of child absence epilepsy with T-STAR gene]Yu-cai Chen, Yue-hua Zhang, Jian-jun Lü, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|October 15, 2013
[Clinical and genetic characteristics of glucose transporter type 1 deficiency syndrome]Yan-yan Liu, Xin-hua Bao, Shuang Wang, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|June 1, 2005
[Clinical and laboratory screening studies on urea cycle defects]Yan-ling Yang, Fang Sun, Ning Qian, et al.
Chinese Medical Journal|March 18, 2006
Clinical and laboratory survey of 65 Chinese patients with Leigh syndromeYan-ling Yang, Fang Sun, Yao Zhang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 3, 2006
[The effect of CACNA1H gene G773D mutation on calcium channel function]Ju-li Wang, Chong-yang Han, Yu-hong Jing, et al.
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