HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN (HPFH) - RAPID DIAGNOSIS OF DELETIONS INVOLVING THE BETA-GLOBIN GENE BY FLUORESCENCE IN-SITU HYBRIDIZATION (FISH)

被引：0
|
作者：
SHAFFER, LG
NGUYEN, DD
SYLVESTERJACKSON, D
ZHANG, YH
MCCABE, ERB
机构：
[1] BAYLOR COLL MED,INST MOLEC GENET,HOUSTON,TX 77030
[2] BAYLOR COLL MED,DEPT PEDIAT,HOUSTON,TX 77030
来源：
PEDIATRIC RESEARCH | 1994年 / 35卷 / 04期
关键词：
D O I：
暂无
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
引用
收藏
页码：A170 / A170
页数：1
相关论文
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  • [7] A NEW HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN DELETION HAS THE BREAKPOINT WITHIN THE 3' BETA-GLOBIN GENE ENHANCER
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  • [9] 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
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    Prchal, J. T.
    [J]. JOURNAL OF MOLECULAR DIAGNOSTICS, 2010, 12 (06): : 866 - 866
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