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	1.	[WASP gene mutation analysis of a family of X-linked thrombocytopenia]. [electronic resource] by Shi, Rui-Ming Liu, Zhi-Gang Yang, Yong-Hua Producer: 20101216 In: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics vol. 12 Availability: No items available. Save to lists Add to cart (remove)
	2.	[Investigation and OCRL mutation analysis of a family with oculocerebrorenal syndrome of Lowe]. [electronic resource] by Shi, Rui-Ming Bian, Xu-Hua Li, Li-Min Liu, Xiao-Hong Producer: 20140826 In: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	3.	[Site-directed mutagenesis and protein expression of SCN5A gene associated with congenital long QT syndrome]. [electronic resource] by Shi, Rui-Ming Qiang, Hua Zhang, Yan-Min Ma, Ai-Qun Gao, Jie Producer: 20130808 In: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics vol. 15 Availability: No items available. Save to lists Add to cart (remove)
	4.	[Role of transient receptor potential vanilloid 1 in airway inflammation in asthmatic mice]. [electronic resource] by Feng, Shuang Zhang, Yuan-Yuan Gao, Wen-Juan Bian, Xu-Hua Shi, Rui-Ming Producer: 20170202 In: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics vol. 18 Availability: No items available. Save to lists Add to cart (remove)
	5.	Role of the TSLP-DC-OX40L pathway in asthma pathogenesis and airway inflammation in mice. [electronic resource] by Feng, Shuang Zhang, Li Bian, Xu-Hua Luo, Ying Qin, Guang-Hui Shi, Rui-Ming Producer: 20181211 In: Biochemistry and cell biology = Biochimie et biologie cellulaire vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Phenytoin-responsive epileptic encephalopathy with a tandem duplication involving [electronic resource] by Shi, Rui-Ming Kobayashi, Tomoko Kikuchi, Atsuo Sato, Ryo Uematsu, Mitsugu An, Kumiko Kure, Shigeo Publication details: Neurology. Genetics Feb 2017 In: Neurology. Genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Site-directed mutagenesis of neonatal convulsions associated KCNQ2 gene and its protein expression. [electronic resource] by Zhou, Xi-Hui Hui, Zhi-Yan Shi, Rui-Ming Song, Hong-Xia Zhang, Wei Liu, Li Producer: 20160202 In: Translational pediatrics vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	[Site-directed mutagenesis and protein expression of KCNQ2 gene associated with neonatal convulsions]. [electronic resource] by Zhou, Xi-Hui Hui, Zhi-Yan Shi, Rui-Ming Song, Hong-Xia Zhang, Wei Liu, Li Producer: 20111006 In: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	9.	[A novel mutation in KCNQ2 gene causes benign familial infantile convulsions (BFIC) in a Chinese family]. [electronic resource] by Zhou, Xi-hui Ma, Ai-qun Liu, Xiao-hong Huang, Chen Zhang, Yan-min Shi, Rui-ming Producer: 20100726 In: Zhonghua er ke za zhi = Chinese journal of pediatrics vol. 44 Availability: No items available. Save to lists Add to cart (remove)
	10.	[Linkage analysis and gene mapping of one Chinese family with benign familial infantile convulsions]. [electronic resource] by Zhou, Xi-Hui Ma, Ai-Qun Liu, Xiao-Hong Huang, Chen Zhang, Yan-Min Shi, Rui-Ming Producer: 20100518 In: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics vol. 12 Availability: No items available. Save to lists Add to cart (remove)
	11.	[Clinical manifestations and gene mutations of a Chinese family with MYH9-related syndrome]. [electronic resource] by Shi, Rui-Ming Cao, Xiao-Qin Luo, Shu-Fang Fang, Xia-Ling Wang, Rong-Hua Liu, Zhi-Gang Producer: 20130417 In: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	12.	[Gene mutation analysis of a Chinese family of congenital long Q-T syndrome type three]. [electronic resource] by Shi, Rui-ming Ma, Ai-qun Zhang, Yan-min Yang, Chun Huang, Chen Zhou, Xi-hui Liu, Xiao-hong Producer: 20110104 In: Zhonghua er ke za zhi = Chinese journal of pediatrics vol. 47 Availability: No items available. Save to lists Add to cart (remove)