HEMOGLOBIN BARTS HYDROPS SYNDROME IN GREECE

被引:12
作者
KATTAMIS, C
METAXOTOUMAVROMATI, A
TSIARTA, E
METAXATOU, C
WASI, P
WOOD, WG
PRESSLEY, L
HIGGS, DR
CLEGG, JB
WEATHERALL, DJ
机构
[1] SIRIRAJ HOSP,DEPT MED,BANGKOK,THAILAND
[2] JOHN RADCLIFFE HOSP,MRC,NUFFIELD DEPT CLIN MED,MOLEC HAEMATOL UNIT,OXFORD OX3 9DU,ENGLAND
关键词
D O I
10.1136/bmj.281.6235.268
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:268 / 270
页数:3
相关论文
共 14 条
[1]   CASE OF INTRAUTERINE DEATH DUE TO ALPHA-THALASSAEMIA [J].
DIAMOND, MP ;
COTGROVE, I ;
PARKER, A .
BRITISH MEDICAL JOURNAL, 1965, 2 (5456) :278-&
[2]  
KAN YW, 1979, BLOOD, V54, P1434
[3]   GENETICAL INTERPRETATION OF HAEMOGLOBIN-H DISEASE [J].
KATTAMIS, C ;
LEHMANN, H .
HUMAN HEREDITY, 1970, 20 (02) :156-&
[4]   THE CHROMOSOMAL ARRANGEMENT OF HUMAN ALPHA-LIKE GLOBIN GENES - SEQUENCE HOMOLOGY AND ALPHA-GLOBIN GENE DELETIONS [J].
LAUER, J ;
SHEN, CKJ ;
MANIATIS, T .
CELL, 1980, 20 (01) :119-130
[5]   DUPLICATED HUMAN ALPHA-GLOBIN GENES LIE CLOSE TOGETHER IN CELLULAR DNA [J].
ORKIN, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1978, 75 (12) :5950-5954
[6]   GENE DELETION AS CAUSE OF ALPHA THALASSEMIA - SEVERE FORM OF ALPHA THALASSEMIA IS CAUSED BY A HEMOGLOBIN GENE DELETION [J].
OTTOLENGHI, S ;
LANYON, WG ;
PAUL, J ;
WILLIAMSON, R ;
WEATHERALL, DJ ;
CLEGG, JB ;
PRITCHARD, J ;
POOTRAKUL, S ;
BOON, WH .
NATURE, 1974, 251 (5474) :389-392
[7]  
PATARYAS HA, 1972, BLOOD-J HEMATOL, V39, P688, DOI 10.1182/blood.V39.5.688.688
[8]  
PRESSLEY L, P NATL ACAD SCI US
[9]   K562 HUMAN-LEUKEMIC CELLS SYNTHESIZE EMBRYONIC HEMOGLOBIN IN RESPONSE TO HEMIN [J].
RUTHERFORD, TR ;
CLEGG, JB ;
WEATHERALL, DJ .
NATURE, 1979, 280 (5718) :164-165
[10]   HEMOGLOBIN BARTS HYDROPS FETALIS SYNDROME IN AN INFANT OF GREEK ORIGIN AND PRENATAL DIAGNOSIS OF ALPHA-THALASSEMIA [J].
SHARMA, RS ;
YU, V ;
WALTERS, WAW .
MEDICAL JOURNAL OF AUSTRALIA, 1979, 2 (08) :404-&