The molecular basis for the phenotypic differences between delta beta-thalassemia and HPFH: The role of the two silencers upstream of the delta-globin gene.

被引：0
|
作者：
Kosteas, T
Moschonas, N
Anagnou, NP
机构：
[1] UNIV CRETE,SCH MED,IRAKLION,GREECE
[2] INST MOL BIOL & BIOTECHNOL,IRAKLION,GREECE
来源：
BLOOD | 1996年 / 88卷 / 10期
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
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页码：587 / 587
页数：1
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  • [11] The molecular basis of beta-thalassemia intermedia - The conjunction of defects in both beta and alpha-globin gene loci.
    Chen, J
    Liu, WP
    Sheng, M
    Chen, MJ
    Huang, SZ
    Zeng, YT
    [J]. BLOOD, 1995, 86 (10) : 2566 - 2566
  • [12] HETEROCELLULAR HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN (HPFH) - MOLECULAR MECHANISMS OF ABNORMAL GAMMA-GENE EXPRESSION IN ASSOCIATION WITH BETA-THALASSEMIA AND LINKAGE RELATIONSHIP WITH THE BETA-GLOBIN GENE-CLUSTER
    GIAMPAOLO, A
    MAVILIO, F
    SPOSI, NM
    CARE, A
    MASSA, A
    CIANETTI, L
    PETRINI, M
    RUSSO, R
    CAPPELLINI, MD
    MARINUCCI, M
    [J]. HUMAN GENETICS, 1984, 66 (2-3) : 151 - 156
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