HEMOGLOBIN-A2 IN IRON DEFICIENT BETA-THALASSEMIA HETEROZYGOTES

被引：25

作者：

GALANELLO, R

RUGGERI, R

ADDIS, M

PAGLIETTI, E

CAO, A

机构：

来源：

HEMOGLOBIN | 1981年 / 5卷 / 06期

关键词：

D O I：

10.3109/03630268108991694

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：

引用

页码：613 / 618

页数：6

共 7 条

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[2]

EFREMOV DG, 1977, HEMOGLOBINOPATHIES T, P281

[3] BETA-THALASSEMIA TRAIT IN SARDINIA [J].

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MELIS, MA ;

RUGGERI, R ;

ADDIS, M ;

SCALAS, MT ;

MACCIONI, L ;

FURBETTA, M ;

ANGIUS, A ;

TUVERI, T ;

CAO, A .

HEMOGLOBIN, 1979, 3 (01) :33-46

[4]

HUISMAN THJ, 1975, J LAB CLIN MED, V86, P700

[5] SERUM IRON AND UNSATURATED IRON-BINDING CAPACITY IN THE BETA-THALASSEMIA TRAIT - THEORETIC RELATION TO LEVELS OF HEMOGLOBIN-A, HAEMOGLOBIN-A-2, AND HEMOGLOBIN-F [J].

KATTAMIS, C ;

LAGOS, P ;

MATSANIOTIS, N ;

METAXOTO.A .

JOURNAL OF MEDICAL GENETICS, 1972, 9 (02) :154-+

[6]

LAUBER K, 1965, Z KLIN CHEM KLIN BIO, V3, P96

[7]

WASI P, 1968, J LAB CLIN MED, V71, P85

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