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	1.	[Effects of early environment on the expression of brain-derived neurotrophic factor and its receptor and brain development]. [electronic resource] by Chen, Jin-Lan Chen, Yan-Hui 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)
	2.	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)
	3.	Clinical and molecular delineation of 16p13.3 duplication in a patient with congenital heart defect and multiple congenital anomalies. [electronic resource] by Chen, Jin-Lan Yang, Yi-Feng Huang, Can Wang, Jian Yang, Jin-Fu Tan, Zhi-Ping Producer: 20120604 In: American journal of medical genetics. Part A vol. 158A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Rare copy number variations containing genes involved in RASopathies: deletion of SHOC2 and duplication of PTPN11. [electronic resource] by Chen, Jin-Lan Zhu, Xin Zhao, Tian-Li Wang, Jian Yang, Yi-Feng Tan, Zhi-Ping Producer: 20140812 In: Molecular cytogenetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Congenital heart defect and mental retardation in a patient with a 13q33.1-34 deletion. [electronic resource] by Huang, Can Yang, Yi-Feng Yin, Ni Chen, Jin-Lan Wang, Jian Zhang, Hong Tan, Zhi-Ping Producer: 20120529 In: Gene vol. 498 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	[Multifactor analysis of postoperative mechanical ventilation supporting time in infants with congenital heart diseases]. [electronic resource] by Chen, Jin-Lan Yang, Yi-Feng Hu, Jian-Guo Yin, Bang-Liang Gong, Qi-Hua Xu, Xin-Hua Producer: 20080421 In: Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences vol. 32 Availability: No items available. Save to lists Add to cart (remove)
	7.	One-stage correction of aortic coarctation and severe mitral regurgitation via left posteriolateral thoracotomy in a 2-year-old child. [electronic resource] by Gong, Qi Hua Yang, Yi Feng Zhao, Tian Li Yang, Jin Fu Wu, Zhong Shi Chen, Jin Lan Yin, Ni Producer: 20081016 In: Journal of cardiac surgery vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Whole-exome sequencing identifies Y1495X of SCN5A to be associated with familial conduction disease and sudden death. [electronic resource] by Tan, Zhi-Ping Xie, Li Deng, Yao Chen, Jin-Lan Zhang, Wei-Zhi Wang, Jian Yang, Jin-Fu Yang, Yi-Feng Producer: 20151028 In: Scientific reports vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	A 1.1Mb deletion in distal 13q deletion syndrome region with congenital heart defect and postaxial polydactyly: additional support for a CHD locus at distal 13q34 region. [electronic resource] by Yang, Yi-Feng Ai, Qi Huang, Can Chen, Jin-Lan Wang, Jian Xie, Li Zhang, Wei-Zhi Yang, Jin-Fu Tan, Zhi-Ping Producer: 20131113 In: Gene vol. 528 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Duplication of 10q22.3-q23.3 encompassing BMPR1A and NGR3 associated with congenital heart disease, microcephaly, and mild intellectual disability. [electronic resource] by Tang, Mi Yang, Yi-Feng Xie, Li Chen, Jin-Lan Zhang, Wei-Zhi Wang, Jian Zhao, Tian-Li Yang, Jin-Fu Tan, Zhi-Ping Producer: 20161020 In: American journal of medical genetics. Part A vol. 167A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Microduplication of 3p25.2 encompassing RAF1 associated with congenital heart disease suggestive of Noonan syndrome. [electronic resource] by Luo, Cheng Yang, Yi-Feng Yin, Bang-Liang Chen, Jin-Lan Huang, Can Zhang, Wei-Zhi Wang, Jian Zhang, Hong Yang, Jin-Fu Tan, Zhi-Ping Producer: 20121105 In: American journal of medical genetics. Part A vol. 158A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Duplication of 8q12 encompassing CHD7 is associated with a distinct phenotype but without duane anomaly. [electronic resource] by Luo, Hong Xie, Li Wang, Shou-Zheng Chen, Jin-Lan Huang, Can Wang, Jian Yang, Jin-Fu Zhang, Wei-Zhi Yang, Yi-Feng Tan, Zhi-Ping Producer: 20130218 In: European journal of medical genetics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Rare de novo copy number variants in patients with congenital pulmonary atresia. [electronic resource] by Xie, Li Chen, Jin-Lan Zhang, Wei-Zhi Wang, Shou-Zheng Zhao, Tian-Li Huang, Can Wang, Jian Yang, Jin-Fu Yang, Yi-Feng Tan, Zhi-Ping Producer: 20141230 In: PloS one vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)