HOMOZYGOUS BETA THALASSEMIA IN LIBERIA

被引：20

作者：

WILLCOX, MC ^{[1
]}

WEATHERALL, DJ ^{[1
]}

CLEGG, JB ^{[1
]}

机构：

[1] UNIV LIVERPOOL,DEPT HEMATOL,LIVERPOOL L69 3BX,LANCASHIRE,ENGLAND

来源：

JOURNAL OF MEDICAL GENETICS | 1975年 / 12卷 / 02期

关键词：

D O I：

10.1136/jmg.12.2.165

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：165 / 173

页数：9

共 26 条

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[13] THALASSEMIA MAJOR WITH COMPLETE SUPPRESSION OF HBA PRODUCTION IN GHANAIAN GIRL [J].

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[14]

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[15]

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[16]

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[17] STUDIES ON ABNORMAL HEMOGLOBINS .1. THEIR DEMONSTRATION IN SICKLE CELL ANEMIA AND OTHER HEMATOLOGIC DISORDERS BY MEANS OF ALKALI DENATURATION [J].

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CHERNOFF, AI ;

SINGER, L .

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[18]

STIJNS J, 1956, Ann Soc Belg Med Trop (1920), V36, P763

[19]

VANDEPITTE J, 1959, ABNORMAL HAEMOGLOBIN, P271

[20]

WATSONWILLIAMS EJ, 1965, ABNORMAL HAEMOGLOBIN, P233

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