Hb S-Hb Monroe;: A sickle cell β-thalassemia syndrome

被引：2

作者：

Sweeting, I ^{[1
]}

Serjeant, BE

Serjeant, GR

Kulozik, AE

Vetter, B

机构：

[1] Univ W Indies, MRC Labs, Kingston 7, Jamaica

[2] Humboldt Univ, Zentrum Kinder & Jugendmed, D-13353 Berlin, Germany

来源：

HEMOGLOBIN | 1998年 / 22卷 / 02期

关键词：

D O I：

10.3109/03630269809092139

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：

[No abstract available]

引用

页码：153 / 156

页数：4

共 6 条

[1] ESTIMATION OF SMALL PERCENTAGES OF FOETAL HAEMOGLOBIN [J].

BETKE, K ;

MARTI, HR ;

SCHLICHT, I .

NATURE, 1959, 184 (4702) :1877-1878

[2] HB-MONROE OR ALPHA-2-BETA-230(B12)ARG-]THR, A VARIANT ASSOCIATED WITH BETA-THALASSEMIA DUE TO A G-]C SUBSTITUTION ADJACENT TO THE DONOR SPLICE SITE OF THE 1ST INTRON [J].

GONZALEZREDONDO, JM ;

STOMING, TA ;

KUTLAR, F ;

KUTLAR, A ;

HU, H ;

WILSON, JB ;

HUISMAN, THJ .

HEMOGLOBIN, 1989, 13 (01) :67-74

[3] COMPARISON OF HEMATOLOGICAL FEATURES OF BETA0 AND BETA+ THALASSEMIA TRAITS IN JAMAICAN NEGROES [J].

MILLARD, DP ;

MASON, K ;

SERJEANT, BE ;

SERJEANT, GR .

BRITISH JOURNAL OF HAEMATOLOGY, 1977, 36 (02) :161-170

[4] A SIMPLE AND RAPID METHOD OF DIRECT SEQUENCING USING DYNABEADS [J].

THEIN, SL ;

HINTON, J .

BRITISH JOURNAL OF HAEMATOLOGY, 1991, 79 (01) :113-115

[5] Beta-thalassaemia in the immigrant and non-immigrant German populations [J].

Vetter, B ;

Schwarz, C ;

Kohne, E ;

Kulozik, AE .

BRITISH JOURNAL OF HAEMATOLOGY, 1997, 97 (02) :266-272

[6] A 5' SPLICE-REGION G -] C MUTATION IN EXON 1 OF THE HUMAN BETA-GLOBIN GENE INHIBITS PRE-MESSENGER RNA SPLICING - A MECHANISM FOR BETA+-THALASSEMIA [J].

VIDAUD, M ;

GATTONI, R ;

STEVENIN, J ;

VIDAUD, D ;

AMSELEM, S ;

CHIBANI, J ;

ROSA, J ;

GOOSSENS, M .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (03) :1041-1045

← 1 →