ALPHA- AND BETA-THALASSEMIA IN THAILAND

被引：205
作者：
WASI, P
NANAKORN, S
POOTRAKUL, SN
SOOKANEK, M
DISTHASONGCHAN, P
PORNPATKUL, M
PANICH, V
机构：
[1] Division of Hematology, Department of Medicine, Siriraj Hospital Medical School, Bangkok
来源：
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES | 1969年 / 165卷 / A1期
关键词：
D O I：
10.1111/j.1749-6632.1969.tb27777.x
中图分类号：
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号：
07 ; 0710 ; 09 ;
摘要：
[No abstract available]
引用
收藏
页码：60 / +
页数：1
相关论文
共 85 条
[1]  
AKSOY M., 1959, ACTA HAEMATOL, V22, P188
[2]   THALASSAEMIA SYNDROMES .1. THALASSAEMIA MINOR WITH LARGE AMOUNT OF FETAL HAEMOGLOBIN - STUDY OF A FAMILY [J].
AKSOY, M ;
EGRIBOZLU, A ;
ALPUSTUN, H .
ACTA HAEMATOLOGICA, 1961, 25 (02) :136-+
[3]  
Aksoy Muzafffer, 1959, ABNORMAL HAEMOGLOBIN, P216
[4]   SICKLING OF ERYTHROCYTES IN A PATIENT WITH THALASSEMIA-HEMOGLOBIN-I DISEASE [J].
ATWATER, J ;
SCHWARTZ, IR ;
ERSLEV, AJ ;
MONTGOMERY, TL ;
TOCANTINS, LM .
NEW ENGLAND JOURNAL OF MEDICINE, 1960, 263 (24) :1215-1223
[5]   PROPERTIES OF HAEMOGLOBIN H + THEIR SIGNIFICANCE IN RELATION TO FUNCTION OF HAEMOGLOBIN [J].
BENESCH, R ;
BENESCH, RE .
NATURE, 1964, 202 (493) :773-&
[6]  
BENESCH RE, 1961, J BIOL CHEM, V236, P2926
[7]  
BERNINI L, 1962, ACTA GENET STAT MED, V12, P202
[8]  
BETKE K, 1958, Blut, V4, P241, DOI 10.1007/BF01630321
[9]  
BHAMARAPRAVATI N, 1967, AM J CLIN PATHOL, V47, P745
[10]   HOMOZYGOUS BETA DELTA THALASSAEMIA (BETA DELTA MICROCYTHAEMIA) [J].
BRANCATI, C ;
BAGLIONI, C .
NATURE, 1966, 212 (5059) :262-&
123456789