SCREENING FOR THALASSEMIA TRAIT BY ELECTRONIC MEASUREMENT OF MEAN CORPUSCULAR VOLUME

被引:99
作者
PEARSON, HA [1 ]
OBRIEN, RT [1 ]
MCINTOSH, S [1 ]
机构
[1] YALE UNIV,SCH MED,DEPT PEDIAT,NEW HAVEN,CT 06510
关键词
D O I
10.1056/NEJM197302152880706
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:351 / 353
页数:3
相关论文
共 13 条
[1]   COMPREHENSIVE SCREENING PROGRAM FOR HEMOGLOBINOPATHIES [J].
BARNES, MG ;
KOMARMY, L ;
NOVACK, AH .
JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1972, 219 (06) :701-&
[2]  
CROSBY WH, 1972, BLOOD, V39, P298
[3]   THE DIAGNOSIS OF THALASSEMIA TRAIT BY STARCH BLOCK ELECTROPHORESIS OF THE HEMOGLOBIN [J].
GERALD, PS ;
DIAMOND, LK .
BLOOD, 1958, 13 (01) :61-69
[4]  
HARRIS JW, 1970, RED CELL PRODUCTION, P117
[5]   GLOBIN CHAIN SYNTHESIS IN ALPHA THALASSEMIA SYNDROMES [J].
KAN, YW ;
SCHWARTZ, E ;
NATHAN, DG .
JOURNAL OF CLINICAL INVESTIGATION, 1968, 47 (11) :2515-&
[6]   NEW HEMOGLOBIN IN NORMAL ADULT BLOOD [J].
KUNKEL, HG ;
WALLENIUS, G .
SCIENCE, 1955, 122 (3163) :288-288
[7]   TYPES OF THALASSAEMIA-TRAIT CARRIERS AS REVEALED BY A STUDY OF THEIR INCIDENCE IN GREECE [J].
MALAMOS, B ;
FESSAS, P ;
STAMATOYANNOPOULOS, G .
BRITISH JOURNAL OF HAEMATOLOGY, 1962, 8 (01) :5-+
[8]  
ROSE MS, 1971, BRIT MED J, V2, P169
[9]   SILENT CARRIER OF BETA THALASSEMIA [J].
SCHWARTZ, E .
NEW ENGLAND JOURNAL OF MEDICINE, 1969, 281 (24) :1327-&
[10]   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