Characterization of a New α-Thalassemia-1 Mutation in a Spanish Family-Reference-Cited by-同舟云学术

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Characterization of a New α-Thalassemia-1 Mutation in a Spanish Family

Published:1994-01 Issue:1 Volume:18 Page:29-37
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Villegas A.,Sanchez J.,Ricard P.,Gonzalez F. A.,Potro E. Del,Armada B.,Carreno D. L.,Espinos D.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269409014143

Reference16 articles.

1. The chromosomal arrangement of human α-like globin genes: Sequence homology and α-globin gene deletions

2. A review of the molecular genetics of the human alpha-globin gene cluster

3. Characterisation of a new α thalassemia 1 defect due to a partial deletion of the α globin gene complex

4. A new gene deletion involving the α2-, α1 -, and 81-globin genes in a black family with Hb H disease

Cited by 12 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. Alpha-Thalassemia in Southern Italy: Characterization of Five New Deletions Removing the Alpha-Globin Gene Cluster;International Journal of Molecular Sciences;2023-01-30

2. Caracterización molecular de dos nuevas mutaciones de α° talasemia en 2 familias españolas (mutación --ED y --GP);Medicina Clínica;2011-05

3. 0 Thalassaemia as a result of a novel 11.1 kb deletion eliminating both of the duplicated globin genes;Journal of Clinical Pathology;2004-02-01

4. THE THALASSEMIA SYNDROMES: MOLECULAR CHARACTERIZATION IN THE SPANISH POPULATION;Hemoglobin;2001-01

5. 2 α-Thalassaemia;Baillière's Clinical Haematology;1998-03

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