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	Title	Author(s)	Issue Date	Views
	Exome sequencing reveals a heterozygous DLX5 mutation in a Chinese family with autosomal-dominant split-hand/foot malformation Journal:European Journal of Human Genetics	Wang, X Xin, Q Li, L Li, J Zhang, C Qiu, R Qian, C Zhao, H Liu, Y Shan, H Dang, J Bian, X Shao, C Gong, Y Liu, Q	2014	36
	A Missense Mutation in SLC33A1, which Encodes the Acetyl-CoA Transporter, Causes Autosomal-Dominant Spastic Paraplegia (SPG42) Journal:American Journal of Human Genetics	Lin, P Li, J Liu, Q Mao, F Li, J Qiu, R Hu, H Song, Y Yang, Y Gao, G Yan, C Yang, W Shao, C Gong, Y	2008	302
	A novel deletion mutation in GJB1 causes X-linked Charcot-Marie-Tooth disease in a Han Chinese family Journal:Muscle and Nerve	Lin, P Mao, F Liu, Q Yang, W Shao, C Yan, C Gong, Y	2010	148

Showing results 1 to 3 of 3