Clinical and whole-exome sequencing findings in two siblings from Hani ethnic minority with congenital glycosylation disorders by Zhen Zhang, Ti-Long Huang, Jing Ma, Wen-Ji He, Huaiyu Gu

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A de novo ANK1 mutation associated to hereditary spherocytosis: a case report by Ti-Long Huang, Bao-Hua Sang, Qing-Ling Lei, Chun-Yan Song, Yun-Bi Lin, Yu Lv, Chun-Hui Yang, Na Li, Yue-Huang Yang, Xian-Wen Zhang, Xin Tian

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Gene Mutation Spectrum of Thalassemia Among Children in Yunnan Province by Ti-Long Huang, Tian-Yao Zhang, Chun-Yan Song, Yun-Bi Lin, Bao-Hua Sang, Qing-Ling Lei, Yu Lv, Chun-Hui Yang, Na Li, Xin Tian, Yue-Huang Yang, Xian-Wen Zhang

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