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World Journal of Pediatrics : WJP|August 9, 2015
Clinical characteristics of hemolytic uremic syndrome secondary to cobalamin C disorder in Chinese childrenQi-Liang Li, Wen-Qi Song, Xiao-Xia Peng, et al.
Yi Chuan Xue Bao = Acta Genetica Sinica|October 6, 2005
[Detection of germline mutations in the APC gene with the protein truncation test]Xiao-Rong Liu, Xiang-Nian Shan, W Friedl, et al.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. Acta Academiae Medicinae Sinicae|December 3, 2003
[Translocation between chromosomes 4q35 and 10q26 in facioscapulohumeral muscular dystrophy]Quan-xi Su, Cheng Zhang, Ying Zeng, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 12, 2004
[Application of the Bgl II-Bln I dosage test to gene diagnosis of facioscapulohumeral muscular dystrophy 1A gene]Quan-xi Su, Cheng Zhang, You-mei Xie, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 12, 2003
[Large deletion in mismatch repair genes uncovered by quantitative multiplex PCR-high performance liquid chromatography system]Ya-ping Wang, Ming Zhu, Meng-hong Sun, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 10, 2004
[The detection of microsatellite instability by ion-pair reversed-phase high performance liquid chromatography]Xiao-rong Liu, Ya-ping Wang, Jun-ni Zhang, et al.
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