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	21.	Whole exome sequencing identifies a novel mutation (c.333 + 2T > C) of TNNI3K in a Chinese family with dilated cardiomyopathy and cardiac conduction disease. [electronic resource] by Fan, Liang-Liang Huang, Hao Jin, Jie-Yuan Li, Jing-Jing Chen, Ya-Qin Zhao, Shui-Ping Xiang, Rong Producer: 20180226 In: Gene vol. 648 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	A Novel ZRS Mutation in a Chinese Patient with Preaxial Polydactyly and Triphalangeal Thumb. [electronic resource] by Wu, Pan-Feng Guo, Shuai Fan, Xue-Feng Fan, Liang-Liang Jin, Jie-Yuan Tang, Ju-Yu Xiang, Rong Producer: 20170116 In: Cytogenetic and genome research vol. 149 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Whole-Exome Sequencing Identifies Two Novel TTN Mutations in Chinese Families with Dilated Cardiomyopathy. [electronic resource] by Liu, Ji-Shi Fan, Liang-Liang Zhang, Hao Liu, Xiaoxian Huang, Hao Tao, Li-Jian Xia, Kun Xiang, Rong Producer: 20180802 In: Cardiology vol. 136 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Identification of a novel mutation of NOG in family with proximal symphalangism and early genetic counseling. [electronic resource] by Ma, Cong Liu, Lv Wang, Fang-Na Tian, Hai-Shen Luo, Yan Yu, Rong Fan, Liang-Liang Li, Ya-Li Producer: 20200214 In: BMC medical genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Whole-exome sequencing identifies a Novel SCN5A mutation (C335R) in a Chinese family with arrhythmia. [electronic resource] by Huang, Hao Ding, Dong-Bo Fan, Liang-Liang Jin, Jie-Yuan Li, Jing-Jing Guo, Shuai Chen, Ya-Qin Xiang, Rong Producer: 20180910 In: Cardiology in the young vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Novel mutations of low-density lipoprotein receptor gene in China patients with familial hypercholesterolemia. [electronic resource] by Fan, Liang-liang Lin, Min-jie Chen, Ya-qin Huang, Hao Peng, Dao-quan Xia, Kun Zhao, Shui-ping Xiang, Rong Producer: 20160211 In: Applied biochemistry and biotechnology vol. 176 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	A novel proximal 3q29 chromosome microdeletion in a Chinese patient with Chiari malformation type II and Sprengel's deformity. [electronic resource] by Guo, Shuai Fan, Xue-Feng Jin, Jie-Yuan Fan, Liang-Liang Zeng, Lei Zhou, Zheng-Bing Xiang, Rong Tang, Ju-Yu Publication details: Molecular cytogenetics 2018 In: Molecular cytogenetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Compound heterozygous [electronic resource] by Yu, Fang Jin, Jie-Yuan He, Ji-Qiang Fan, Liang-Liang Jiao, Zi-Jun Wu, Pan-Feng Tang, Ju-Yu Xiang, Rong Publication details: International journal of clinical and experimental pathology 2019 In: International journal of clinical and experimental pathology vol. 12 Availability: No items available. Save to lists Add to cart (remove)
	29.	A Novel Heterozygous Variant in F2 Gene in a Chinese Patient With Coronary Thrombosis and Acute Myocardial Infarction Leads to Antithrombin Resistance. [electronic resource] by Tang, Yi Zhang, Liyang Xie, Wenlin Jin, Jieyuan Luo, Yujiao Deng, Mingyang Liu, Zhengyu Pan, Hong Wei Zhang, Yi Zheng, Zhaofen Fan, Liang-Liang Publication details: Frontiers in genetics 2020 In: Frontiers in genetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Mutation detection in Chinese patients with familial hypercholesterolemia. [electronic resource] by Du, Ran Fan, Liang-Liang Lin, Min-Jie He, Zhi-Jian Huang, Hao Chen, Ya-Qin Li, Jing-Jing Xia, Kun Zhao, Shui-Ping Xiang, Rong Publication details: SpringerPlus 2016 In: SpringerPlus vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Increased Reticulon 3 (RTN3) Leads to Obesity and Hypertriglyceridemia by Interacting With Heat Shock Protein Family A (Hsp70) Member 5 (HSPA5). [electronic resource] by Xiang, Rong Fan, Liang-Liang Huang, Hao Chen, Ya-Qin He, Wanxia Guo, Shuai Li, Jing-Jing Jin, Jie-Yuan Du, Ran Yan, Riqiang Xia, Kun Producer: 20190930 In: Circulation vol. 138 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	A novel splice-site mutation of WRN (c.IVS28+2T>C) identified in a consanguineous family with Werner Syndrome. [electronic resource] by Wu, Pan-Feng Jin, Jie-Yuan Li, Jing-Jing He, Ji-Qiang Fan, Liang-Liang Jin, Min Huang, Hao Xia, Kun Tang, Ju-Yu Xiang, Rong Producer: 20180305 In: Molecular medicine reports vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	A mutation of beta-tropomyosin gene in a Chinese family with distal arthrogryposis type I. [electronic resource] by Jin, Jie-Yuan Wu, Pan-Feng Fan, Liang-Liang Yu, Fang Li, Jing-Jing Fan, Xue-Feng Huang, Hao Zeng, Lei Tang, Ju-Yu Xiang, Rong Publication details: International journal of clinical and experimental pathology 2017 In: International journal of clinical and experimental pathology vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	34.	The genetic spectrum of familial hypercholesterolemia in the central south region of China. [electronic resource] by Xiang, Rong Fan, Liang-Liang Lin, Min-Jie Li, Jing-Jing Shi, Xiang-Yu Jin, Jie-Yuan Liu, Yu-Xing Chen, Ya-Qin Xia, Kun Zhao, Shui-Ping Producer: 20171120 In: Atherosclerosis vol. 258 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)