Haematological phenotypes in a family with triplicated α-globin gene, β∘39 and δ+27 thalassaemia mutations-Reference-Cited by-同舟云学术

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Haematological phenotypes in a family with triplicated α-globin gene, β∘39 and δ+27 thalassaemia mutations

Published:2008-06-28 Issue:4 Volume:14 Page:289-292
ISSN:0141-9854
Container-title:Clinical & Laboratory Haematology
language:en
Short-container-title:

Author:

OGGIANO LINA,RIMINI ELENA,FROGHERI LAURA,GUISO LUCIANA,PISTIDDA PAOLA,LONGINOTTI MAURIZIO

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2257.1992.tb00104.x/fullpdf

Reference8 articles.

1. A benign form of thalassaemia intermedia may be determined by the interaction of triplicated α locus and heterozygous β-thalassaemia.;CAMASCHELLA;Br. J. Haem.,1987

2. Hematological characteristics of the β-thalassaemia in Sardinian children.;GALANELLO;J. Clin. Pathol.,1980

3. α globin gene triplication in severe heterozygous β-thalassemia.;HENNI;Acta Haemat,1985

4. Thalassaemia intermedia: interaction of the triple α-globin gene arrangement and heterozygous β-thalassaemia.;KULOZIK;Br. J. Haem.,1987

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A 12-year preventive program for β-thalassemia in Northern Sardinia;Clinical Genetics;2008-06-28

2. A novel mediterranean “δβ-thalassemia” determinant containing the δ+27 and β°39 point mutations in cis;American Journal of Hematology;1994-01

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