MEDITERRANEAN ANEMIA IN THE NEGRO - A RE-EVALUATION OF 4 PATIENTS AND THEIR FAMILIES

被引:14
作者
SCHWARTZ, SO
HARTZ, WH
机构
关键词
D O I
10.1182/blood.V10.12.1256.1256
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:1256 / 1266
页数:11
相关论文
共 9 条
[1]  
BARKAN GEORG, 1940, JOUR BIOL CHEM, V135, P37
[2]   HEMOGLOBIN-C DISEASE - REPORT OF 4 CASES [J].
HARTZ, WH ;
SCHWARTZ, SO .
BLOOD, 1955, 10 (03) :235-246
[3]   A NEW INHERITED ABNORMALITY OF HUMAN HEMOGLOBIN [J].
ITANO, HA ;
NEEL, JV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1950, 36 (11) :613-617
[4]   A NEW INHERITED ABNORMALITY OF HEMOGLOBIN AND ITS INTERACTION WITH SICKLE CELL HEMOGLOBIN [J].
KAPLAN, E ;
ZUELZER, WW ;
NEEL, JV .
BLOOD, 1951, 6 (12) :1240-1259
[5]   ELECTROPHORESIS OF PROTEINS ON FILTER PAPER [J].
KUNKEL, HG ;
TISELIUS, A .
JOURNAL OF GENERAL PHYSIOLOGY, 1951, 35 (01) :89-118
[6]   MEDITERRANEAN ANEMIA IN THE NEGRO - A REPORT OF 4 CASES AND THEIR FAMILIES [J].
SCHWARTZ, SO ;
MASON, J .
BLOOD, 1949, 4 (06) :706-721
[7]   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
[8]   STUDIES ON ABNORMAL HEMOGLOBINS .10. A NEW SYNDROME - HEMOGLOBIN-C-THALASSEMIA DISEASE [J].
SINGER, K ;
KRAUS, AP ;
SINGER, L ;
RUBINSTEIN, HM ;
GOLDBERG, SR .
BLOOD, 1954, 9 (11) :1032-1046
[9]  
SPAET T, 1953, J PEDIAT, V12, P483