HAEMOGLOBIN H DISEASE IN ARABS IN KUWAIT

被引:6
作者
ALI, SA
机构
关键词
D O I
10.1136/jcp.22.2.226
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
[No abstract available]
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页码:226 / &
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共 14 条
[1]   HAEMOGLOBINOPATHIES IN IMMIGRANT FAMILIES [J].
BEARD, MJ ;
SIGNY, AG .
POSTGRADUATE MEDICAL JOURNAL, 1965, 41 (480) :624-&
[2]   STUDIES ON THALASSAEMIA-LIKE ANAEMIAS IN PREGNANT IMMIGRANTS IN LONDON [J].
BEAVEN, GH ;
DIXON, G ;
WHITE, JC .
BRITISH JOURNAL OF HAEMATOLOGY, 1966, 12 (06) :777-&
[3]  
Dacie J.V., 1991, PRACTICAL HAEMATOLOG, P54
[4]  
GOUTTAS A, 1955, Sang, V26, P911
[5]   THALASSAEMIA TYPES AMONG KURDISH JEWS IN ISRAEL [J].
HOROWITZ, A ;
COHEN, T ;
GOLDSCHMIDT, E ;
LEVENE, C .
BRITISH JOURNAL OF HAEMATOLOGY, 1966, 12 (05) :555-+
[6]   CHEMICAL CHARACTERIZATION AND SUBUNIT HYBRIDIZATION OF HUMAN HEMOGLOBIN H AND ASSOCIATED COMPOUNDS [J].
JONES, RT ;
SCHROEDER, WA .
BIOCHEMISTRY, 1963, 2 (06) :1357-&
[7]  
LEHMANN H, 1966, MANS HAEMOGLOBINS, P268
[8]  
LEHMANN H, 1966, MANS HAEMOGLOBINS, P176
[9]   GENETIC AND HAEMATOLOGICAL SIGNIFICANCE OF HAEMOGLOBIN-H [J].
MOTULSKY, AG .
NATURE, 1956, 178 (4541) :1055-1056
[10]   HAEMOGLOBIN H DISEASE WITH PERSISTENT HAEMOGLOBIN BARTS IN AN ORIENTAL JEWESS AND HER DAUGHTER - A DUAL ALPHA-CHAIN DEFICIENCY OF HUMAN HAEMOGLOBIN [J].
RAMOT, B ;
SHEBA, C ;
FISHER, S ;
AGER, JAM ;
LEHMANN, H .
BRITISH MEDICAL JOURNAL, 1959, 2 (DEC5) :1228-1230