Abnormal hemoglobin anti-Lepore Hong Kong compound with β0-thalassemia ameliorate thalassemia severity when co-inherited with α-thalassemia
Bao, Xiuqin, Wang, Jicheng, Qin, Danqing, Yao, Cuize, Liang, Jie, Liang, Kailing, Du, Li
Published in Scientific reports (20.03.2024)
Published in Scientific reports (20.03.2024)
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Journal Article
Identification of four novel large deletions and complex variants in the α-globin locus in Chinese population
Bao, Xiuqin, Wang, Jicheng, Qin, Danqing, Yao, Cuize, Liang, Jie, Liang, Kailing, Zeng, Yukun, Du, Li
Published in Human genomics (25.04.2023)
Published in Human genomics (25.04.2023)
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Journal Article
Two novel deletion mutations in β-globin gene cause β-thalassemia trait in two Chinese families
Bao, Xiuqin, Qin, Danqing, Wang, Jicheng, Chen, Jing, Yao, Cuize, Liang, Jie, Liang, Kailing, Wang, Yixia, Wang, Yousheng, Du, Li, Yin, Aihua
Published in Human genomics (08.12.2023)
Published in Human genomics (08.12.2023)
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Journal Article
The -α3.7III subtype of α+-thalassemia was identified in China
Bao, Xiuqin, Wang, Jicheng, Qin, Danqing, Zhang, Rui, Yao, Cuize, Liang, Jie, Liang, Kailing, Du, Li
Published in Hematology (Luxembourg) (01.12.2022)
Published in Hematology (Luxembourg) (01.12.2022)
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Journal Article
The -α 3.7III subtype of α + -thalassemia was identified in China
Bao, Xiuqin, Wang, Jicheng, Qin, Danqing, Zhang, Rui, Yao, Cuize, Liang, Jie, Liang, Kailing, Du, Li
Published in Hematology (Luxembourg) (31.12.2022)
Published in Hematology (Luxembourg) (31.12.2022)
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Journal Article
Abnormal hemoglobin anti-Lepore Hong Kong compound with β 0 -thalassemia ameliorate thalassemia severity when co-inherited with α-thalassemia
Bao, Xiuqin, Wang, Jicheng, Qin, Danqing, Yao, Cuize, Liang, Jie, Liang, Kailing, Du, Li
Published in Scientific reports (20.03.2024)
Get full text
Published in Scientific reports (20.03.2024)
Journal Article