DELTA BETA-THALASSEMIA AND HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN

被引：68

作者：

BOLLEKENS, JA ^{[1
]}

FORGET, BG ^{[1
]}

机构：

[1] YALE UNIV, SCH MED, DEPT HUMAN GENET, NEW HAVEN, CT 06510 USA

来源：

HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA | 1991年 / 5卷 / 03期

关键词：

D O I：

10.1016/S0889-8588(18)30422-2

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

引用

页码：399 / 422

页数：24

共 163 条

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[2]

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[3]

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[4]

ANAND R, 1988, BLOOD, V72, P636

[5]

[Anonymous], 1986, HEMOGLOBIN MOL GENET

[6] THE HUMAN BETA-GLOBIN GENE CONTAINS MULTIPLE REGULATORY REGIONS - IDENTIFICATION OF ONE PROMOTER AND 2 DOWNSTREAM ENHANCERS [J].

ANTONIOU, M ;

DEBOER, E ;

HABETS, G ;

GROSVELD, F .

EMBO JOURNAL, 1988, 7 (02) :377-384

[7]

ATWEH GF, 1986, BLOOD, V68, P1108

[8]

ATWEH GF, 1987, BLOOD, V70, P1470

[9] FUSION OF 2 PEPTIDE CHAINS IN HEMOGLOBIN LEPORE AND ITS INTERPRETATION AS A GENETIC DELETION [J].

BAGLIONI, C .

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[10] MUTUALLY EXCLUSIVE INTERACTION OF THE CCAAT-BINDING FACTOR AND OF A DISPLACEMENT PROTEIN WITH OVERLAPPING SEQUENCES OF A HISTONE GENE PROMOTER [J].

BARBERIS, A ;

SUPERTIFURGA, G ;

BUSSLINGER, M .

CELL, 1987, 50 (03) :347-359

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