MOLECULAR PATHOLOGY OF HEMOGLOBIN-H DISEASE IN SARDINIANS

被引：27

作者：

PAGLIETTI, E ^{[1
]}

GALANELLO, R ^{[1
]}

MOI, P ^{[1
]}

PIRASTU, M ^{[1
]}

CAO, A ^{[1
]}

机构：

[1] UNIV CAGLIARI,IST CLIN & BIOL ETA EVOLUTIVA,VIA JENNER,I-09100 CAGLIARI,ITALY

来源：

BRITISH JOURNAL OF HAEMATOLOGY | 1986年 / 63卷 / 03期

关键词：

D O I：

10.1111/j.1365-2141.1986.tb07525.x

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：485 / 496

页数：12

共 40 条

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[2] DETECTION OF SICKLE-CELL BETA-S-GLOBIN ALLELE BY HYBRIDIZATION WITH SYNTHETIC OLIGONUCLEOTIDES
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[3] ORGANIZATION OF THE ALPHA-GLOBIN GENES IN THE CHINESE ALPHA-THALASSEMIA SYNDROMES
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[4] 2 DIFFERENT MOLECULAR ORGANIZATIONS ACCOUNT FOR THE SINGLE ALPHA-GLOBIN GENE OF THE ALPHA-THALASSEMIA-2 GENOTYPE
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[J]. JOURNAL OF CLINICAL INVESTIGATION, 1980, 66 (06) : 1319 - 1325
[5] ALPHA-THALASSEMIA IN SARDINIAN NEWBORNS
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[J]. BRITISH JOURNAL OF HAEMATOLOGY, 1984, 58 (02) : 361 - 368
[6] PHENOTYPE-GENOTYPE CORRELATION IN HEMOGLOBIN-H DISEASE IN CHILDHOOD
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CAO, A
[J]. JOURNAL OF MEDICAL GENETICS, 1983, 20 (06) : 425 - 429
[7] ALPHA-THALASSEMIA IN SARDINIAN INFANTS
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DIANA, G
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ANGIUS, A
MELIS, MA
ROSATELLI, C
CAO, A
[J]. JOURNAL OF MEDICAL GENETICS, 1980, 17 (05) : 357 - 362
[8] GLOBIN STRUCTURAL MUTANT ALPHA-125 LEU-]PRO IS A NOVEL CAUSE OF ALPHA-THALASSEMIA
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[J]. NATURE, 1982, 296 (5860) : 864 - 865
[9] Goossens M, 1981, Methods Enzymol, V76, P805
[10] Higgs D R, 1983, Curr Top Hematol, V4, P37

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