The Molecular Defects of α-Thalassemia in the Filipino-Reference-Cited by-同舟云学术

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The Molecular Defects of α-Thalassemia in the Filipino

Published:1977-01 Issue:6 Volume:1 Page:539-546
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Dozy A. M.,Kabisch H.,Baker J.,Koenig H. M.,Kurachi S.,Stamatoyannopoulos G.,Todd D.,Kan Y. W.

Publisher

Informa UK Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630267709003418

Reference15 articles.

1. Gene deletion as the cause of α thalassaemia: The severe form of α thalassaemia is caused by a haemoglobin gene deletion

2. Gene deletion as the cause of α thalassaemia: Genetic lesion in homozygous α thalassaemia (hydrops fetalis)

3. Relative numbers of human globin genes assayed with purified alpha and beta complementary human DNA.

4. Deletion of α-globin genes in haemoglobin-H disease demonstrates multiple α-globin structural loci

Cited by 6 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. Characterization of two deletions that remove the entire human ζ-α globin gene complex (—THAIand —FIL);British Journal of Haematology;1988-10

2. Hemoglobin H Disease from Algeria: Genetic and Molecular Characterization;Acta Haematologica;1981

3. alpha-Thalassaemia in Sardinian infants.;Journal of Medical Genetics;1980-10-01

4. Modification of Hemoglobin H Disease by Sickle Trait;Journal of Clinical Investigation;1979-10-01

5. Quantitative studies of hb bart’s levels and red cell indices in alpha thalassaemia trait in mediterraneans;Pathology;1979

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