THE DIAGNOSIS OF THALASSEMIA TRAIT BY STARCH BLOCK ELECTROPHORESIS OF THE HEMOGLOBIN

被引：173

作者：

GERALD, PS

DIAMOND, LK

机构：

来源：

BLOOD | 1958年 / 13卷 / 01期

关键词：

D O I：

10.1182/blood.V13.1.61.61

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：61 / 69

页数：9

共 20 条

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[2]

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[6] A FAMILY ILLUSTRATING THE DOUBLE INHERITANCE OF THE SICKLE CELL TRAIT AND OF MEDITERRANEAN ANAEMIA [J].

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JOURNAL OF CLINICAL PATHOLOGY, 1954, 7 (03) :201-208

[7]

JOSEPHSON A, 1957, MAY C HEM NAT RES CO

[8] FURTHER STUDIES ON HEMOGLOBIN-C .2. THE HEMATOLOGIC EFFECTS OF HEMOGLOBIN-C ALONE AND IN COMBINATION WITH SICKLE CELL HEMOGLOBIN [J].

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ZUELZER, WW ;

NEEL, JV .

BLOOD, 1953, 8 (08) :735-746

[9]

KAPLAN E, 1950, J LAB CLIN MED, V36, P517

[10] NEW HEMOGLOBIN IN NORMAL ADULT BLOOD [J].

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SCIENCE, 1955, 122 (3163) :288-288

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