HOMOZYGOUS BETA DELTA-THALASSAEMIA - DESCRIPTION OF A CASE AND REVIEW OF LITERATURE

被引：13

作者：

TSISTRAKIS, GA

AMARANTOS, SP

KONKOURIS, LL

机构：

[1] UNIV SALONICA, DEPT HAEMATOL, MED CLIN B, SALONICA, GREECE

[2] 424 GEN MILITARY HOSP, MED CLIN, SALONICA, GREECE

来源：

ACTA HAEMATOLOGICA | 1974年 / 51卷 / 03期

关键词：

D O I：

10.1159/000208292

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：185 / 191

页数：7

共 26 条

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BAGLIONI, C .

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[2] ABSENCE OF CIS DELTA CHAIN SYNTHESIS IN (DELTA BETA) THALASSEMIA (F-THALASSEMIA) [J].

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MOTULSKY, AG .

BLOOD-THE JOURNAL OF HEMATOLOGY, 1966, 28 (01) :54-&

[3] HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN - A STUDY OF 79 AFFECTED PERSONS IN 15 NEGRO FAMILIES IN BALTIMORE [J].

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CHARACHE, S ;

WEATHERALL, DJ ;

SHEPARD, MK ;

RICHARDSON, SN .

BLOOD, 1963, 21 (03) :261-+

[4] HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN IN GREECE . STUDY + COMPARISON [J].

FESSAS, P ;

STAMATOYANNOPOULOS, G .

BLOOD, 1964, 24 (03) :223-&

[5] ABSENCE OF HAEMOGLOBIN A2 IN AN ADULT [J].

FESSAS, P ;

STAMATOYANNOPOULOS, G .

NATURE, 1962, 195 (4847) :1215-&

[6]

Fessas P., 1961, HAEMOGLOBIN COLLOQUI, P90

[7]

FESSAS P, 1968, GENETICS

[8]

FISHER B, 1957, AM J CLIN PATHOL, V27, P48

[9]

FRASER GR, 1964, ANN NY ACAD SCI, V119, P415

[10] THALASSEMIA TRAIT - GENETIC COMBINATIONS OF INCREASED FETAL + A2 HEMOGLOBINS [J].

GABUZDA, TG ;

GARDNER, FH ;

NATHAN, DG .

NEW ENGLAND JOURNAL OF MEDICINE, 1964, 270 (23) :1212-&

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