Hb Chad or α223(B4)GLU→LYSβ2Observed in Members of a Surinam Family in Association with α-Thalassemia-2 and with HB S-Reference-Cited by-同舟云学术

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Hb Chad or α223(B4)GLU→LYSβ2Observed in Members of a Surinam Family in Association with α-Thalassemia-2 and with HB S

Published:1989-01 Issue:6 Volume:13 Page:543-556
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Codrington J. F.,Codrington F. A.,Wisse J. H.,Wilson J. B.,Webber B. B.,Wong S. C.,Huisman T. H. J.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630268908993105

Reference25 articles.

1. Hemoglobin Chad [α23 (B4) Glu → Lys] Discovered in a Japanese with Questionable Polycythemia

Cited by 11 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. Hb Fulton-Georgia [α20(B1)His→Pro;HBA1: c.62A>C]: A New α-Globin Variant Coinherited with α-Thalassemia-2 (3.7 kb deletion) and Hb SC Disease;Hemoglobin;2013-07-03

2. International Hemoglobin Information Center Variant List;Hemoglobin;1997-01

3. Variants of the Alpha Chain;Hemoglobin;1996-01

4. The differences in quantities of α2-and α1-globin gene variants in heterozygotes;British Journal of Haematology;1994-10

5. International Hemoglobin Information Center;Hemoglobin;1994-01

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