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	1.	Whole-Exome Sequencing Identifies a Novel Mutation of Desmocollin 2 in a Chinese Family With Arrhythmogenic Right Ventricular Cardiomyopathy. [electronic resource] by Liu, Ji-Shi Fan, Liang-Liang Li, Jing-Jing Xiang, Rong Producer: 20170425 In: The American journal of cardiology vol. 119 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A passive microfluidic device for continuous microparticle enrichment. [electronic resource] by Fan, Liang-Liang Zhu, Xiao-Liang Yan, Qing Zhe, Jiang Zhao, Liang Producer: 20191227 In: Electrophoresis vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Whole exome sequencing identified a novel mutation (p.Ala1884Pro) of β-spectrin in a Chinese family with hereditary spherocytosis. [electronic resource] by Fan, Liang-Liang Liu, Ji-Shi Huang, Hao Du, Ran Xiang, Rong Producer: 20200406 In: The journal of gene medicine vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Whole-exome sequencing identifies a novel mutation of DSG2 (Y198C) in a Chinese arrhythmogenic right ventricular cardiomyopathy patient. [electronic resource] by Xiang, Rong Fan, Liang-Liang Huang, Hao Zhao, Shui-Ping Chen, Ya-Qin Producer: 20170718 In: International journal of cardiology vol. 214 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Continuous size-based separation of microparticles in a microchannel with symmetric sharp corner structures. [electronic resource] by Fan, Liang-Liang He, Xu-Kun Han, Yu Du, Li Zhao, Liang Zhe, Jiang Producer: 20140416 In: Biomicrofluidics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A Novel Mutation of FOXC1 (R127L) in an Axenfeld-Rieger Syndrome Family with Glaucoma and Multiple Congenital Heart Diseases. [electronic resource] by Du, Rui-Feng Huang, Hao Fan, Liang-Liang Li, Xiang-Ping Xia, Kun Xiang, Rong Producer: 20160914 In: Ophthalmic genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	A novel variant in TBX20 (p.D176N) identified by whole-exome sequencing in combination with a congenital heart disease related gene filter is associated with familial atrial septal defect. [electronic resource] by Liu, Ji-jia Fan, Liang-liang Chen, Jin-lan Tan, Zhi-ping Yang, Yi-feng Producer: 20150622 In: Journal of Zhejiang University. Science. B vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Identification of a compound heterozygous mutation of ABCC2 in a patient with hyperbilirubinemia. [electronic resource] by Xiang, Rong Li, Jing-Jing Fan, Liang-Liang Jin, Jie-Yuan Xia, Kun Wang, Fang Producer: 20180510 In: Molecular medicine reports vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Microduplication of 10q26.3 in a Chinese hypertriglyceridemia patient. [electronic resource] by Li, Jing-Jing Chen, Ya-Qin Fan, Liang-Liang Jin, Jie-Yuan Guo, Shuai Xiang, Rong Producer: 20190125 In: Molecular and cellular probes vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Whole-Exome Sequencing Identifies a Novel Mutation (p.L320R) of Alpha-Actinin 2 in a Chinese Family with Dilated Cardiomyopathy and Ventricular Tachycardia. [electronic resource] by Fan, Liang-Liang Huang, Hao Jin, Jie-Yuan Li, Jing-Jing Chen, Ya-Qin Xiang, Rong Producer: 20190513 In: Cytogenetic and genome research vol. 157 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Enhanced viscoelastic focusing of particle in microchannel. [electronic resource] by Fan, Liang-Liang Zhao, Zhi Tao, Yi-Yi Wu, Xu Yan, Qing Zhe, Jiang Zhao, Liang Producer: 20210322 In: Electrophoresis vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Long-term follow-up of an Alport syndrome patient with a novel mutation of [electronic resource] by Xiang, Rong Li, Jing-Jing Liu, Ji-Shi Fan, Liang-Liang Li, Lin Xia, Kun Zhang, Hao 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)
	13.	Whole-exome sequencing reveals doubly novel heterozygous Myosin Binding Protein C and Titin mutations in a Chinese patient with severe dilated cardiomyopathy. [electronic resource] by Fan, Liang-Liang Chen, Ya-Qin Huang, Hao Jin, Jie-Yuan Li, Jing-Jing Tan, Zhi-Ping Producer: 20190315 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)
	14.	Exome sequencing identifies a novel nonsense mutation of Ring Finger Protein 207 in a Chinese family with Long QT syndrome and syncope. [electronic resource] by Fan, Liang-Liang Chen, Ya-Qin Huang, Hao Yuan, Zhuang-Zhuang Jin, Jie-Yuan Hu, Min Xiang, Rong Producer: 20190410 In: Journal of human genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Microduplications of 10q24 Detected in Two Chinese Patients with Split-hand/foot Malformation Type 3. [electronic resource] by Xiang, Rong Du, Ran Guo, Shuai Jin, Jie-Yuan Fan, Liang-Liang Tang, Ju-Yu Zhou, Zheng-Bing Producer: 20180727 In: Annals of clinical and laboratory science vol. 47 Availability: No items available. Save to lists Add to cart (remove)
	16.	Whole Exome Sequencing Identified a 13 Base Pair [electronic resource] by Fan, Liang-Liang Guo, Shuai Jin, Jie-Yuan He, Zhi-Jian Zhao, Shui-Ping Xiang, Rong Zhao, Wang Producer: 20200622 In: Annals of clinical and laboratory science vol. 49 Availability: No items available. Save to lists Add to cart (remove)
	17.	Whole-exome sequencing identifies a novel mutation of GPD1L (R189X) associated with familial conduction disease and sudden death. [electronic resource] by Huang, Hao Chen, Ya-Qin Fan, Liang-Liang Guo, Shuai Li, Jing-Jing Jin, Jie-Yuan Xiang, Rong Producer: 20190429 In: Journal of cellular and molecular medicine vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	A de novo mutation of SMYD1 (p.F272L) is responsible for hypertrophic cardiomyopathy in a Chinese patient. [electronic resource] by Fan, Liang-Liang Ding, Dong-Bo Huang, Hao Chen, Ya-Qin Jin, Jie-Yuan Xia, Kun Xiang, Rong Producer: 20191120 In: Clinical chemistry and laboratory medicine vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	A novel mutation of GATA4 (K319E) is responsible for familial atrial septal defect and pulmonary valve stenosis. [electronic resource] by Xiang, Rong Fan, Liang-Liang Huang, Hao Cao, Bei-Bei Li, Xiang-Ping Peng, Dao-Quan Xia, Kun Producer: 20140417 In: Gene vol. 534 Availability: No items available. Save to lists Add to cart (remove)
	20.	A novel heterozygous variant p.(Trp538Arg) of SYNM is identified by whole-exome sequencing in a Chinese family with dilated cardiomyopathy. [electronic resource] by Zhang, Shu-Bing Liu, Yu-Xing Fan, Liang-Liang Huang, Hao Li, Jing-Jing Jin, Jie-Yuan Xiang, Rong Producer: 20200220 In: Annals of human genetics vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 34 results.