HB Hradec Kralove (HB HK) or α2β2115(617)ALA→ASP, A Severely Unstable Hewglobin Variant Resulting in a Dominant β-Thalassemia Trait in a Czech Family-Reference-Cited by-同舟云学术

HB Hradec Kralove (HB HK) or α2β2115(617)ALA→ASP, A Severely Unstable Hewglobin Variant Resulting in a Dominant β-Thalassemia Trait in a Czech Family

Published:1993-01 Issue:4 Volume:17 Page:319-328
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Divoky V.,Svobodova M.,Indrak K.,Chrobak L.,Molchanova T. P.,Huisman T. H. J.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269308997485

Reference18 articles.

1. DOMINANT Î² THALASSAEMIA: MOLECULAR BASIS AND PATHOPHYSIOLOGY

2. Righetti P. G., Gianazza E., Bianchi-Bosisio A., Cossu G. The Hemoglobinopathies, Methods on Hematology, T. H.J. Huisman. Churchill Livingstone, Edinburgh 1986; Vol. 15: 47

3. High-performance liquid chromatographic separation of human haemoglobins

4. Fetal hemoglobin in normal adults and ?-thalassemia heterozygotes

5. High Performance Liquid Cbromatographic Separation of Globin Chains on a Large-Pore C4Column

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