HEMOGLOBIN SYNTHESIS STUDIES OF A FAMILY WITH ALPHA-THALASSEMIA TRAIT AND SICKLE-CELL TRAIT

被引：18

作者：

SHAEFFER, JR ^{[1
]}

DESIMONE, J ^{[1
]}

KLEVE, LJ ^{[1
]}

机构：

[1] UNIV TEXAS,MD ANDERSON HOSP & TUMOR INST,CANC CTR,DEPT BIOL,HOUSTON,TX 77025

来源：

BIOCHEMICAL GENETICS | 1975年 / 13卷 / 11-1期

关键词：

D O I：

10.1007/BF00484410

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：783 / 788

页数：6

共 22 条

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[3] UNBALANCED GLOBIN CHAIN SYNTHESIS IN RETICULOCYTES OF SICKLE-CELL TRAIT INDIVIDUALS WITH LOW CONCENTRATIONS OF HEMOGLOBIN-S
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[4] DESIMONE J, 1974, J LAB CLIN MED, V84, P517
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[7] IMPROVED METHOD FOR ESTIMATION OF SMALL QUANTITIES OF ALKALI-RESISTANT HEMOGLOBIN IN BLOOD
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[8] GENETIC DETERMINATION OF PHENOTYPIC VARIATION IN SICKLE-CELL TRAIT
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[10] GENE DELETION AS CAUSE OF ALPHA THALASSEMIA - SEVERE FORM OF ALPHA THALASSEMIA IS CAUSED BY A HEMOGLOBIN GENE DELETION
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[J]. NATURE, 1974, 251 (5474) : 389 - 392

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