ALPHA-THALASSEMIA-2 AND THE VARIABILITY OF HEMATOLOGICAL VALUES IN CHILDREN WITH SICKLE-CELL-ANEMIA

被引：20

作者：

ALTAY, C ^{[1
]}

GRAVELY, ME ^{[1
]}

JOSEPH, BR ^{[1
]}

WILLIAMS, DF ^{[1
]}

机构：

[1] MED COLL GEORGIA,DEPT PEDIAT,AUGUSTA,GA 30901

来源：

PEDIATRIC RESEARCH | 1981年 / 15卷 / 08期

关键词：

D O I：

10.1203/00006450-198115080-00004

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：1093 / 1096

页数：4

共 15 条

[1]

ABRAHAM EC, 1977, HEMOGLOBIN, V1, P27

[2] SICKLE-CELL ANEMIA AND TRAIT IN SOUTHERN INDIA - FURTHER-STUDIES [J].

BRITTENHAM, G ;

LOZOFF, B ;

HARRIS, JW ;

MAYSON, SM ;

MILLER, A ;

HUISMAN, THJ .

AMERICAN JOURNAL OF HEMATOLOGY, 1979, 6 (02) :107-123

[3]

Bruning JL, 1977, COMPUTATIONAL HDB ST

[4] ALPHA-GLOBIN GENE ORGANIZATION IN BLACKS PRECLUDES THE SEVERE FORM OF ALPHA-THALASSEMIA [J].

DOZY, AM ;

KAN, YW ;

EMBURY, SH ;

MENTZER, WC ;

WANG, WC ;

LUBIN, B ;

DAVIS, JR ;

KOENIG, HM .

NATURE, 1979, 280 (5723) :605-607

[5] ASSOCIATION OF SICKLE-CELL ANEMIA WITH HETEROZYGOUS AND HOMOZYGOUS ALPHA-THALASSEMIA-2 - INVITRO HB CHAIN SYNTHESIS [J].

FELICE, AE ;

WEBBER, B ;

MILLER, A ;

MAYSON, SM ;

HARRIS, HF ;

HENSON, JB ;

GRAVELY, ME ;

HUISMAN, THJ .

AMERICAN JOURNAL OF HEMATOLOGY, 1979, 6 (02) :91-106

[6] SICKLE-CELL SYNDROMES .2. SICKLE-CELL ANEMIA-ALPHA-THALASSEMIA SYNDROME [J].

HONIG, GR ;

KOSHY, M ;

MASON, RG ;

VIDA, LN .

JOURNAL OF PEDIATRICS, 1978, 92 (04) :556-561

[7] TRIMODALITY IN PERCENTAGES OF BETA-CHAIN VARIANTS IN HETEROZYGOTES - EFFECT OF NUMBER OF ACTIVE HB-ALPHA STRUCTURAL LOCI [J].

HUISMAN, THJ .

HEMOGLOBIN, 1977, 1 (04) :349-382

[8] SICKLE-CELL ANEMIA AS A SYNDROME - REVIEW OF DIAGNOSTIC FEATURES [J].

HUISMAN, THJ .

AMERICAN JOURNAL OF HEMATOLOGY, 1979, 6 (02) :173-184

[9]

Huisman THJ, 1977, HEMOGLOBINOPATHIES T

[10] HEMOGLOBIN CHAIN RECOMBINATION AND THE PATTERN OF COMPOSITION OF HEMOGLOBIN-S AND HEMOGLOBIN-D IN HETEROZYGOTES [J].

OGUNMOLA, GB ;

ESAN, GJF ;

FALUSI, AG .

ACTA HAEMATOLOGICA, 1980, 63 (02) :94-100

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