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1.A strong association of the SNP rs** with wet earwax and bromhidrosis in a Chinese family 2013.8 Journal of genetics2.X-Linked Congenital Hypertrichosis Syndrome Is Associated with Interchromosomal Insertions Mediated by a Human-Specific Palindrome near SOX3.£¨Ó°ÏìÒò×Ó11.68£©£¨µÚÒ»×÷Õߣ© 2011.6 American Journal of Human Genetics3.Xp22.3 microdeletions in three Chinese families with X-linked ichthyosis.£¨µÚÒ»×÷Õߣ© 2009.3 Journal of dermatological science4.Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis. 2009.6 Nature genetics5.Copy-number mutations on chromosome 17q24.2-q24.3 in congenital generalized hypertrichosis terminalis with or without gingival hyperplasia. 2009.4 American Journal of Human Genetics6.Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract. 2009.7 Human Mutation.7.Three novel mutations of the EDA gene in Chinese patients with X-linked hypohidrotic ectodermal dysplasia.. 2009.8 British Journal of Dermatology