BETA-THALASSEMIA

被引：58

作者：

THEIN, SL ^{[1
]}

机构：

[1] JOHN RADCLIFFE HOSP, INST MOLEC MED, MRC, MOLEC HAEMATOL UNIT, OXFORD OX3 9DU, ENGLAND

来源：

BAILLIERES CLINICAL HAEMATOLOGY | 1993年 / 6卷 / 01期

关键词：

D O I：

10.1016/S0950-3536(05)80069-1

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：151 / 175

页数：25

共 98 条

[1] ISOLATION AND CHARACTERIZATION OF THE TRANSLATION PRODUCT OF A BETA-GLOBIN GENE NONSENSE MUTATION (BETA-121 GAA-]TAA) [J].

ADAMS, JG ;

STEINBERG, MH ;

KAZAZIAN, HH .

BRITISH JOURNAL OF HAEMATOLOGY, 1990, 75 (04) :561-567

[2] HEMOGLOBIN INDIANAPOLIS (BETA-112[G14] ARGININE) - UNSTABLE BETA-CHAIN VARIANT PRODUCING THE PHENOTYPE OF SEVERE BETA-THALASSEMIA [J].

ADAMS, JG ;

BOXER, LA ;

BAEHNER, RL ;

FORGET, BG ;

TSISTRAKIS, GA ;

STEINBERG, MH .

JOURNAL OF CLINICAL INVESTIGATION, 1979, 63 (05) :931-938

[3]

[Anonymous], 1986, HEMOGLOBIN MOL GENET

[4]

BAKLOUTI F, 1986, BLOOD, V67, P957

[5] INCREASED PROTEIN-BINDING TO A-530 MUTATION OF THE HUMAN BETA-GLOBIN GENE ASSOCIATED WITH DECREASED BETA-GLOBIN SYNTHESIS [J].

BERG, PE ;

MITTELMAN, M ;

ELION, J ;

LABIE, D ;

SCHECHTER, AN .

AMERICAN JOURNAL OF HEMATOLOGY, 1991, 36 (01) :42-47

[6]

BERIS P, 1988, BLOOD, V72, P801

[7] THE SPECTRUM OF BETA-THALASSEMIA IN BURMA [J].

BROWN, JM ;

THEIN, SL ;

WEATHERALL, DJ ;

MAR, KM .

BRITISH JOURNAL OF HAEMATOLOGY, 1992, 81 (04) :574-578

[8] THE HOMOZYGOUS STATE FOR THE -87C-]G-BETA+ THALASSEMIA [J].

CAMASCHELLA, C ;

ALFARANO, A ;

GOTTARDI, E ;

SERRA, A ;

REVELLO, D ;

SAGLIO, G .

BRITISH JOURNAL OF HAEMATOLOGY, 1990, 75 (01) :132-133

[9] INTERACTION BETWEEN HOMOZYGOUS BETA-0-THALASSEMIA AND THE SWISS TYPE OF HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN [J].

CAPPELLINI, MD ;

FIORELLI, G ;

BERNINI, LF .

BRITISH JOURNAL OF HAEMATOLOGY, 1981, 48 (04) :561-572

[10]

CHEHAB FF, 1987, BLOOD, V69, P1141

← 1 2 3 4 5 6 7 8 9 10 →