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HAEMOGLOBIN-H DISEASE

被引：24
作者：
BINGLE, JP
HUEHNS, ER
PRANKERD, TAJ
机构：
来源：
BRITISH MEDICAL JOURNAL | 1958年 / 2卷 / DEC6期
关键词：
D O I：
10.1136/bmj.2.5109.1389
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：1389 / 1390
页数：2
相关论文
共 7 条
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[2]  
HARRIS IM, 1957, CLIN SCI, V16, P633
[3]  
JOSKE RA, 1956, CLIN SCI, V15, P511
[4]   GENETIC AND HAEMATOLOGICAL SIGNIFICANCE OF HAEMOGLOBIN-H [J].
MOTULSKY, AG .
NATURE, 1956, 178 (4541) :1055-1056
[5]   NEW HEMOGLOBIN POSSESSING A HIGHER ELECTROPHORETIC MOBILITY THAN NORMAL ADULT HEMOGLOBIN [J].
RIGAS, DA ;
KOLER, RD ;
OSGOOD, EE .
SCIENCE, 1955, 121 (3141) :372-372
[6]   STUDIES ON ABNORMAL HEMOGLOBINS .1. THEIR DEMONSTRATION IN SICKLE CELL ANEMIA AND OTHER HEMATOLOGIC DISORDERS BY MEANS OF ALKALI DENATURATION [J].
SINGER, K ;
CHERNOFF, AI ;
SINGER, L .
BLOOD, 1951, 6 (05) :413-428
[7]   A HAEMOGLOBINOPATHY INVOLVING HAEMOGLOBIN-H AND A NEW (Q) HAEMOGLOBIN [J].
VELLA, F ;
WELLS, RHC ;
AGER, JAM ;
LEHMANN, H .
BMJ-BRITISH MEDICAL JOURNAL, 1958, 1 (MAR29) :752-755
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