GAMMA-CHAIN HETEROGENEITY OF FETAL HEMOGLOBIN IN NON-BLACK BETA-THALASSEMIA AND DELTA-BETA-THALASSEMIA AND HPFH HETEROZYGOTES AND HOMOZYGOTES

被引：14

作者：

EFREMOV, GD

IBARRA, B

GURGEY, A

SUKUMARAN, PK

ALTAY, C

HUISMAN, THJ

机构：

[1] MED COLL GEORGIA, CTR COMPREHENS SICKLE CELL, DEPT CELL & MOLEC BIOL, PROT CHEM LAB, AUGUSTA, GA 30912 USA

[2] HACETTEPE UNIV, HACETTEPE CHILDRENS HOSP, DEPT PEDIAT, ANKARA, TURKEY

[3] TATA MEM CTR, CANC RES INST, BOMBAY 400012, INDIA

[4] AUTOKOMANDA, FAK ZEMJODELSKI, ODDELENIE BIOCHEM, Skopje, YUGOSLAVIA

[5] INST MEXICANO SEGURO SOC, DIV GENET, UNIDAD INVEST BIOMED OCCIDENTE, GUADALAJARA, MEXICO

来源：

AMERICAN JOURNAL OF HEMATOLOGY | 1982年 / 12卷 / 04期

关键词：

D O I：

10.1002/ajh.2830120408

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：367 / 382

页数：16

共 32 条

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[8] NEW HB VARIANT - HB F SARDINIA GAMMA-75 (E 19) ISOLEUCINE -] THREONINE FOUND IN A FAMILY WITH HB G PHILADELPHIA, BETA-CHAIN DEFICIENCY AND A LEPORE-LIKE HEMOGLOBIN INDISTINGUISHABLE FROM HB A2 [J].

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