MOLECULAR-BASIS OF THALASSEMIA

被引：0

作者：

WEATHERALL, DJ ^{[1
]}

机构：

[1] UNIV OXFORD,NUFFIELD COLL,DEPT CLIN MED,OXFORD,ENGLAND

来源：

JOHNS HOPKINS MEDICAL JOURNAL | 1976年 / 139卷 / 05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：

引用

页码：205 / 210

页数：6

共 19 条

[1]

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[4]

FORGET BG, 1975, BLOOD, V46, P1002

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[7] DEMONSTRATION OF NON-FUNCTIONAL BETA-GLOBIN MESSENGER-RNA IN HOMOZYGOUS BETA-DEGREE THALASSEMIA [J].

KAN, YW ;

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[8] DELETION OF BETA-GLOBIN STRUCTURE GENE IN HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN [J].

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[9]

OTTOLENGHI, IN PRESS

[10] GENE DELETION AS CAUSE OF ALPHA THALASSEMIA - SEVERE FORM OF ALPHA THALASSEMIA IS CAUSED BY A HEMOGLOBIN GENE DELETION [J].

OTTOLENGHI, S ;

LANYON, WG ;

PAUL, J ;

WILLIAMSON, R ;

WEATHERALL, DJ ;

CLEGG, JB ;

PRITCHARD, J ;

POOTRAKUL, S ;

BOON, WH .

NATURE, 1974, 251 (5474) :389-392

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