Hasil Pencarian - Cuize Yao

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  1. 1
    First study to describe a novel HbA2: c.400A > C mutation and Hb Dongguan heterozygote in two unrelated Chinese families

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

    Diterbitkan 2022-12-01
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  2. 2
    Hb Q-Thailand heterozygosity unlinked with the (–α4.2/) α+-thalassemia deletion allele identified by long-read SMRT sequencing: hematological and molecular analyses

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

    Diterbitkan 2023-12-01
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  3. 3
    Abnormal hemoglobin anti-Lepore Hong Kong compound with β0-thalassemia ameliorate thalassemia severity when co-inherited with α-thalassemia

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

    Diterbitkan 2024-03-01
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  4. 4
    Compounded with hemoglobin Port Phillip and ‐α4.2 or ‐‐SEA deletions were identified in Chinese population

    Compounded with hemoglobin Port Phillip and ‐α4.2 or ‐‐SEA deletions were identified in Chinese population oleh Li Du, Xiuqin Bao, Danqing Qin, Jicheng Wang, Cuize Yao, Jie Liang, Jianhong Chen, Aihua Yin

    Diterbitkan 2021-09-01
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  5. 5
    Compound heterozygosity for hemoglobin variant Hb-Broomhill and the Southeast Asian α-thalassemia deletion does not worsen outcome: a case report of two unrelated patients

    Compound heterozygosity for hemoglobin variant Hb-Broomhill and the Southeast Asian α-thalassemia deletion does not worsen outcome: a case report of two unrelated patients oleh Danqing Qin, Li Du, Jicheng Wang, Cuize Yao, Hao Guo, Tenglong Yuan, Jie Liang, Aihua Yin

    Diterbitkan 2020-11-01
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  6. 6
    Identification of four novel large deletions and complex variants in the α-globin locus in Chinese population

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

    Diterbitkan 2023-04-01
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  7. 7
    Accurate detection of α-globin gene copy number variants with two reactions using droplet digital PCR

    Accurate detection of α-globin gene copy number variants with two reactions using droplet digital PCR oleh Xiuqin Bao, Danqing Qin, Jian Ma, Xiangcheng Zhou, Jicheng Wang, Cuize Yao, Liang Zhang, Li Du

    Diterbitkan 2022-12-01
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  8. 8
    The -α3.7III subtype of α+-thalassemia was identified in China

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

    Diterbitkan 2022-12-01
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  9. 9
    Hb Chapel Hill or Alpha2 74(EF3) Asp>Gly, a mildly unstable variant found in a Chinese family

    Hb Chapel Hill or Alpha2 74(EF3) Asp>Gly, a mildly unstable variant found in a Chinese family oleh Bin Tang, Jicheng Wang, Danqinq Qin, Cuize Yao, Keyi Chen, Lihua Liang, Huiying Chai, Hao Guo, Li Du

    Diterbitkan 2023-12-01
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  10. 10
    The first Chinese case of unstable Hemoglobin Santa Ana detected by capillary electrophoresis: a case report and literature review

    The first Chinese case of unstable Hemoglobin Santa Ana detected by capillary electrophoresis: a case report and literature review oleh Li Du, Danqing Qin, Jicheng Wang, Cuize Yao, Juan Zhu, Hao Guo, Tenglong Yuan, Jie Liang, Aihua Yin

    Diterbitkan 2022-12-01
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  11. 11
    Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden (:c.178G>C) and Hb Quong Sze (:c.377T>C)

    Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden (:c.178G>C) and Hb Quong Sze (:c.377T>C) oleh Li Du, Xiuqin Bao, Wei He, Danqing Qin, Jicheng Wang, Ying Xiong, Xiaomei Shi, Hongke Ding, Cuize Yao, Jing Wu

    Diterbitkan 2021-07-01
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  12. 12
    Two novel deletion mutations in β-globin gene cause β-thalassemia trait in two Chinese families

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

    Diterbitkan 2023-12-01
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  13. 13
    High positive predictive value of CNVs detected by clinical exome sequencing in suspected genetic diseases

    High positive predictive value of CNVs detected by clinical exome sequencing in suspected genetic diseases oleh 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

    Diterbitkan 2024-07-01
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