ALPHA-BETA THALASSEMIA DISEASE IN A NEGRO FAMILY

被引：25

作者：

PEARSON, HA

机构：

来源：

NEW ENGLAND JOURNAL OF MEDICINE | 1966年 / 275卷 / 04期

关键词：

D O I：

10.1056/NEJM196607282750402

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：176 / &

共 35 条

[1] SICKLE-CELL-THALASSAEMIA DISEASE IN SOUTH TURKEY [J].

AKSOY, M ;

LEHMANN, H .

BRITISH MEDICAL JOURNAL, 1957, 1 (MAR30) :734-738

[2] 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

[3] VARIETY OF HUMAN HEMOGLOBIN WITH 4 DISTINCT ELECTROPHORETIC COMPONENTS [J].

ATWATER, J ;

SCHWARTZ, IR ;

TOCANTINS, LM .

BLOOD, 1960, 15 (06) :901-908

[4]

BERNINI L, 1962, ACTA GENET STAT MED, V12, P202

[5] DETERMINATION OF IRON IN PLASMA OR SERUM [J].

BOTHWELL, TH ;

MALLETT, B .

BIOCHEMICAL JOURNAL, 1955, 59 (04) :599-602

[6] MULTIPLE INHERITED ERYTHROCYTE ABNORMALITIES IN AN AMERICAN NEGRO FAMILY - HEREDITARY SPHEROCYTOSIS, SICKLING AND THALASSEMIA [J].

COHEN, F ;

ZUELZER, WW ;

NEEL, JV ;

ROBINSON, AR .

BLOOD, 1959, 14 (07) :816-827

[7] HUMAN HAPTOGLOBINS - ESTIMATION AND PURIFICATION [J].

CONNELL, GE ;

SMITHIES, O .

BIOCHEMICAL JOURNAL, 1959, 72 :115-&

[8] HAEMOGLOBIN Q-ALPHA-THALASSAEMIA [J].

DORMANDY, KM ;

LOCK, SP ;

LEHMANN, H .

BRITISH MEDICAL JOURNAL, 1961, 1 (523) :1582-&

[9]

FESSAS P, 1962, HAEMOGLOBIN COLLOQUI, P74

[10] THE DIAGNOSIS OF THALASSEMIA TRAIT BY STARCH BLOCK ELECTROPHORESIS OF THE HEMOGLOBIN [J].

GERALD, PS ;

DIAMOND, LK .

BLOOD, 1958, 13 (01) :61-69

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