A New Sickling Disorder Resulting from Interaction of the Genes for Haemoglobin S and α-Thalassaemia
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1969.tb01402.x/fullpdf
Reference17 articles.
1. Observations on the Chromatographic Heterogeneity of Normal Adult and Fetal Human Hemoglobin: A Study of the Effects of Crystallization and Chromatography on the Heterogeneity and Isoleucine Content
2. Rate of Sickling of Red Cells during Deoxygenation of Blood from Persons with Various Sickling Disorders
3. Abnormal human haemoglobins
4. Haemoglobin Synthesis in α-Thalassaemia (Haemoglobin H Disease)
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