Novel mutations in Chinese Han patients with tuberous sclerosis complex: Case series and review of the published work von Zheng, Li‐Yun, LEE, Yu‐Wei, Han, Yang, Tang, Li‐Li, Cheng, Yu‐Yan, Dou, Jin‐Fa, Zhou, Fu‐Sheng, Zheng, Xiao‐Dong, Wang, Hong‐Yan, Wang, Pei‐Guang, Gao, Min

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Association of HLA-DQA1 and DQB1 alleles with keloids in Chinese Hans von Lu, Wen-Sheng, Wang, Jian-Feng, Yang, Sen, Xiao, Feng-Li, Quan, Cheng, Cheng, Hui, Wang, Pei-Guang, Zhang, An-Ping, Cai, Li-Qiong, Zhang, Xue-Jun

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Decreased Serum Level of Interferon-γ in Patients with Pityriasis Rosea von Zeng, Ming, Zhao, Shi-Xiang, Liu, Ling-Hua, Zuo, Xian-Bo, Zheng, Xiao-Dong, Li, Tao, Zhang, Min, Wang, Pei-Guang, Yang, Sen

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A novel U2HR non-synonymous mutation in a Chinese patient with Marie Unna Hereditary Hypotrichosis von Cai, Li-Qiong, Wang, Pei-Guang, Gao, Min, Lu, Wen-Sheng, Xu, Sheng-Xin, Fang, Qiao-Yun, Zhou, Wen-Ming, Lin, Da, Du, Wen-Hui, Zhang, Shu-Mei, Yang, Sen, Zhang, Xue-Jun

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Oscillation Theorems for Even Order Damped Equations with Distributed Deviating Arguments von Gao, Chunxia, Wang, Pei-Guang

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Polymorphisms in Interleukin-15 Gene on Chromosome 4q31.2 Are Associated with Psoriasis Vulgaris in Chinese Population von Zhang, Xue-Jun, Yan, Kai-Lin, Wang, Zhi-Min, Yang, Sen, Zhang, Guo-Long, Fan, Xing, Xiao, Feng-Li, Gao, Min, Cui, Yong, Wang, Pei-Guang, Sun, Liang-dan, Zhang, Kai-Yue, Wang, Beilan, Wang, Da-Zhi, Xu, Shi-Jie, Huang, Wei, Liu, Jian-Jun

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Inversa Acne (Hidradenitis Suppurativa): A Case Report and Identification of the Locus at Chromosome 1p21.1–1q25.3 von Gao, Min, Wang, Pei-Guang, Cui, Yong, Yang, Sen, Zhang, Yu-Hui, Lin, Da, Zhang, Kai-Yue, Liang, Yan-Hua, Sun, Liang-Dan, Yan, Kai-Lin, Xiao, Feng-Li, Huang, Wei, Zhang, Xue-Jun

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Exome sequencing identified a missense mutation of EPS8L3 in Marie Unna hereditary hypotrichosis von Zhang, Xin, Guo, Bi-Rong, Cai, Li-Qiong, Jiang, Tao, Sun, Liang-Dan, Cui, Yong, Hu, Jing-Chu, Zhu, Jun, Chen, Gang, Tang, Xian-Fa, Sun, Guang-Qing, Tang, Hua-Yang, Liu, Yuan, Li, Min, Li, Qi-Bin, Cheng, Hui, Gao, Min, Li, Ping, Yang, Xu, Zuo, Xian-Bo, Zheng, Xiao-Dong, Wang, Pei-Guang, Wang, Jian, Wang, Jun, Liu, Jian-Jun, Yang, Sen, Li, Ying-Rui, Zhang, Xue-Jun

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Association of HLA class I alleles with aloplecia areata in Chinese Hans von Xiao, Feng-Li, Yang, Sen, Yan, Kai-lin, Cui, Yong, Liang, Yan-Hua, Zhou, Fu-Sheng, Du, Wen-Hui, Gao, Min, Sun, Liang-Dan, Fan, Xing, Chen, Jian-Jun, Wang, Pei-Guang, Zhu, Ya-Gang, Zhou, Shun-Ming, Zhang, Xue-Jun

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HLA haplotypic association with different phenotype of alopecia areata in Chinese Hans von Xiao, Feng-Li, Yang, Sen, Lin, Guo-Shu, Gao, Min, Cui, Yong, Yin, Xian-Yong, Wang, Pei-Guang, Xu, Shengxin, Zhang, Xue-Jun

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Oscillation of Second-Order Nonlinear Delay Dynamic Equations with Damping on Time Scales von Agwa, H. A., Khodier, Ahmed M. M., Hassan, Heba A.

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The Gene for a Rare Autosomal Dominant Form of Pompholyx Maps to Chromosome 18q22.1–18q22.3 von Chen, Jian-Jun, Liang, Yan-Hua, Zhou, Fu-Sheng, Yang, Sen, Wang, Jian, Wang, Pei-Guang, Du, Wen-Hui, Xu, Shi-Jie, Huang, Wei, Zhang, Xue-Jun

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Identification of a Novel Locus for Progressive Symmetric Erythrokeratodermia to a 19.02-cM Interval at 21q11.2–21q21.2 von Cui, Yong, Yang, Sen, Gao, Min, Zhou, Wen-Ming, Li, Ming, Wang, Ying, Chen, Jian-Jun, Yan, Kai-Lin, Niu, Zhen-Min, Wang, Pei-Guang, Xiao, Feng-Li, Liang, Yan-Hua, Sun, Liang-Dan, Fan, Xing, Huang, Wei, Zhang, Xue-Jun

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Follow-Up Analysis of PSORS9 in 151 Chinese Families Confirmed the Linkage to 4q31–32 and Refined the Evidence to the Families of Early-Onset Psoriasis von Yan, Kai-Lin, Huang, Wei, Zhang, Xue-Jun, Yang, Sen, Chen, Yu-Ming, Xiao, Feng-Li, Fan, Xing, Gao, Min, Cui, Yong, Zhang, Guo-Long, Sun, Liang-dan, Wang, Pei-Guang, Chen, Jian-Jun, Li, Wei, Chen, Ze-hua, Wang, Zhi-Min, Wang, Da-zhi, Zhang, Kai-Yue, Liu, Jian-Jun

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Existence of Positive Solutions for Second-Order m-Point Boundary Value Problems on Time Scales von Wang, Pei-guang, Wang, Ying

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novel KIT missense mutation in one Chinese family with piebaldism von Yin, Xian-Yong, Ren, Yun-Qing, Yang, Sen, Xu, Sheng-Xin, Zhou, Fu-Sheng, Du, Wen-Hui, Lin, Da, Wang, Pei-Guang, Zhang, Shu-Mei, Zhang, Xue-Jun

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Five mutations of ATP2A2 gene in Chinese patients with Darier's disease and a literature review of 86 cases reported in China von REN, Yun-Qing, MIN GAO, SHEN, Yu-Jun, SEN YANG, ZHANG, Xue-Jun, LIANG, Yan-Hua, HOU, Yan-Xia, WANG, Pei-Guang, SUN, Liang-Dan, XU, Sheng-Xin, WEI LI, DU, Wen-Hui, ZHOU, Fu-Sheng

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Identification of a Novel Locus for Marie Unna Hereditary Hypotrichosis to a 17.5 cM Interval at 1p21.1–1q21.3 von Yang, Sen, Gao, Min, Cui, Yong, Yan, Kai-Lin, Ren, Yun-Qing, Zhang, Guo-Long, Wang, Pei-Guang, Xiao, Feng-Li, Du, Wen-Hui, Liang, Yan-Hua, Sun, Liang-Dan, Xu, Shi-Jie, Huang, Wei, Zhang, Xue-Jun

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A new image fusion algorithm based on fractional wavelet transform von Hua Tian, Pei-guang Wang, Wei Zheng

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A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2 von Wang, Pei-Guang, Gao, Min, Cui, Yong, Xiao, Feng-Li, Zhu, Ya-Gang, Ren, Yun-Qing, Yan, Kai-Lin, Du, Wen-Hui, Zhang, Kai-Yue, Yang, Sen, Huang, Wei, Zhang, Xue-Jun

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