Publications by authors named "Ruo Xiao"

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Whole-exome sequencing identifies a variant in TMEM132E causing autosomal-recessive nonsyndromic hearing loss DFNB99.
Jiangxia Li, Xiaohan Zhao, Qian Xin, Shan Shan, Baichun Jiang, Ruo Xiao, Jingjing Xiao

Hum Mutat· January 2015

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Six mutations in AAGAB confirm its pathogenic role in Chinese punctate palmoplantar keratoderma patients.
Hongzhou Cui, Min Gao, Wenjun Wang, Ruo Xiao, Gang Chen

J Invest Dermatol· November 2013

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Rapid gene identification in a Chinese osteopetrosis family by whole exome sequencing.
Weiguo Sui, Minglin Ou, Jinlong Liang, Min Ding, Jiejing Chen, Ruo Xiao, Xiaohua Meng, Xiaohua Pan

Gene· March 2013

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Loss-of-function mutations in HOXC13 cause pure hair and nail ectodermal dysplasia.
Zhimiao Lin, Quan Chen, Lei Shi, Mingyang Lee, Kathrin A Giehl, Ruo Xiao

Am J Hum Genet· November 2012

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Exome sequencing identifies a COL14A1 mutation in a large Chinese pedigree with punctate palmoplantar keratoderma.
Bi-Rong Guo, Xin Zhang, Gang Chen, Jian-Guo Zhang, Liang-Dan Sun, Ruo Xiao, Xiao-Dong Zheng, Xiao-Guang Zhang

J Med Genet· September 2012

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