檢索結果 - Cuize Yao

First study to describe a novel HbA2: c.400A > C mutation and Hb Dongguan heterozygote in two unrelated Chinese families 由 Cuize Yao, Danqing Qin, Jicheng Wang, Xiuqin Bao, Jie Liang, Li Du

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Hb Q-Thailand heterozygosity unlinked with the (–α4.2/) α+-thalassemia deletion allele identified by long-read SMRT sequencing: hematological and molecular analyses 由 Danqing Qin, Jicheng Wang, Cuize Yao, Xiuqin Bao, Jie Liang, Li Du

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Abnormal hemoglobin anti-Lepore Hong Kong compound with β0-thalassemia ameliorate thalassemia severity when co-inherited with α-thalassemia 由 Xiuqin Bao, Jicheng Wang, Danqing Qin, Cuize Yao, Jie Liang, Kailing Liang, Li Du

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Identification of four novel large deletions and complex variants in the α-globin locus in Chinese population 由 Xiuqin Bao, Jicheng Wang, Danqing Qin, Cuize Yao, Jie Liang, Kailing Liang, Yukun Zeng, Li Du

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The -α3.7III subtype of α+-thalassemia was identified in China 由 Xiuqin Bao, Jicheng Wang, Danqing Qin, Rui Zhang, Cuize Yao, Jie Liang, Kailing Liang, Li Du

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Two novel deletion mutations in β-globin gene cause β-thalassemia trait in two Chinese families 由 Xiuqin Bao, Danqing Qin, Jicheng Wang, Jing Chen, Cuize Yao, Jie Liang, Kailing Liang, Yixia Wang, Yousheng Wang, Li Du, Aihua Yin

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Prevention and control of thalassemia in Guangdong Province, Southern China: insights from an 11-year retrospective study 由 Danqing Qin, Wei He, Jicheng Wang, Juan Zhu, Cuize Yao, Xiuqin Bao, Jie Liang, Yixia Wang, Kailing Liang, Mingyong Luo, Li Du, Jing Wu

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High positive predictive value of CNVs detected by clinical exome sequencing in suspected genetic diseases 由 Yimo Zeng, Hongke Ding, Xingwang Wang, Yanlin Huang, Ling Liu, Li Du, Jian Lu, Jing Wu, Yukun Zeng, Mingqin Mai, Juan Zhu, Lihua Yu, Wei He, Fangfang Guo, Haishan Peng, Cuize Yao, Yiming Qi, Yuan Liu, Fake Li, Jiexia Yang, Rong Hu, Jie Liang, Jicheng Wang, Wei Wang, Yan Zhang, Aihua Yin

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