The Levels of Abnormal Hemoglobin in Persons with Heterozygosities for an a Chain Variant and for β-Thalassemia
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269708997520
Reference22 articles.
1. Trimodality in Tie Percentages of β Chain Variants in Heterozy-Gotes: The Effect of the Number of Aczive HBαStructural Loci
2. Bunn H. F., Forget B. G. Hemoglobin: Molecular, Genetic and Clinical Aspects. W.B. Saunders Company, Philadelphia 1986; 417–421
3. Organization of ?-chain genes among Hb G-Philadelphia heterozygotes in association with Hb S, ?-thalassemia, and ?-thalassemia-2
4. Hb H disease in a Turkish family resulting from the interaction of a deletional α-thalassaemia-1 and a newly discovered poly A mutation
5. Electrostatic interactions in the assembly of haemoglobin
Cited by 1 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 Further Note on the Combination of an α Chain Variant with β-Thalassemia;Hemoglobin;1998-01
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