HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN IN GREECE . STUDY + COMPARISON
HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN IN GREECE . STUDY + COMPARISON
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DOI：
10.1182/blood.v24.3.223.223
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发表时间：
1964-01-01
期刊：
影响因子：
20.3
通讯作者：
STAMATOYANNOPOULOS, G
中科院分区：
文献类型：
--
作者：
FESSAS, P;STAMATOYANNOPOULOS, G
在6个希腊家庭中发现了胎儿血红蛋白的遗传持续性。在8个人有相关的典型β-地中海贫血，血红蛋白A是主要的血红蛋白成分，临床和血液学特征的轻度地中海贫血。
Hereditary persistence of fetal hemoglobin was noted in 6 Greek families. In 8 individuals there was associated typical [beta]-thalassemia, Hb A being the major hemoglobin component, with clinical and hematological features of mild thalassemia.