ASSOCIATION OF β-THALASSEMIA AND Hb Q-THAILAND RESULTING IN A NORMAL Hb A2 VALUE

被引:5
作者
Liao, Can
Li, Jian
Li, Dongzhi
机构
[1] Prenatal Diagnostic Center, Guangzhou Maternal and Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong
[2] Prenatal Diagnostic Center, Guangzhou Maternal and Neonatal Hospital, Guangzhou, Guangdong 510180
关键词
D O I
10.1080/03630260802004186
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We describe a Chinese woman who was assumed to be a Hb Q-Thailand heterozygote, but was later also shown to have beta-thalassemia (beta-thal) with a normal amount of Hb A(2).
引用
收藏
页码:505 / 508
页数:4
相关论文
共 4 条
  • [1] The IVS-II-1 (G → A) β0-thalassemia mutation in cis with HbA2-Troodos [δ116(G18)Arg → Cys (CGC → TGC)] causes a complex prenatal diagnosis in an Iranian family
    Eram, SM
    Azimifar, B
    Abolghasemi, H
    Foulady, P
    Lotfi, V
    Masrouri, M
    Hosseini, M
    Abdolhosseini, A
    Zeinali, S
    [J]. HEMOGLOBIN, 2005, 29 (04) : 289 - 292
  • [2] Prenatal diagnosis of β-thalassemia by reverse dot-blot hybridization in southern China
    Li, Dongzhi
    Liao, Can
    Li, Jian
    Huang, Yining
    Xie, Xingmei
    Wei, Jiaxue
    Wu, Shaoqing
    [J]. HEMOGLOBIN, 2006, 30 (03) : 365 - 370
  • [3] PIRASTU M, 1990, ANN NY ACAD SCI, V612, P90
  • [4] HB Q-THAILAND [ALPHA-74(EF3)ASP-]HIS] - GENE ORGANIZATION, MOLECULAR-STRUCTURE, AND DNA DIAGNOSIS
    ZENG, FY
    FUCHAROEN, S
    HUANG, SZ
    RODGERS, GP
    [J]. HEMOGLOBIN, 1992, 16 (06) : 481 - 491