Haemoglobin H disease due to (- -SEA ) α-globin gene deletion and α2-codon 30 (ΔGAG) mutation: a family study
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2257.2001.00411.x/fullpdf
Reference7 articles.
1. Hydrops fetalis due to an unusual form of Hb H disease;Chan;Blood,1985
2. Molecular defects in Hb H hydrops fetalis;Chan;British Journal of Haematology,1997
3. Chan V. Chan T.K. Todd D. 1988 Different forms of Hb H disease in the Chinese First International Symposium on Thalassemia. Hemoglobin 12,
4. Dominantly transmitted β-thalassemia arising from the production of several aberrant mRNA species and one abnormal peptide;Faustino;Blood,1998
5. Molecular characterization of severe α-thalassemias causing hydrops fetalis in Taiwan;Ko;American Journal of Medical Genetics,1991
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2. Clinical and Haematological Parameters of Commonly Reported Non-deletional α-thalassaemia Mutations in Southeast Asia: A Review;Malaysian Journal of Medicine and Health Sciences;2022-09-15
3. CODON 30 (–GAG) (α2): Hematological Parameters in Heterozygotes and also Patients with Hb H Disease;Hemoglobin;2013-07-04
4. A laboratory strategy for genotyping haemoglobin H disease in the Chinese;Journal of Clinical Pathology;2006-10-17
5. Hemoglobin H disease: not necessarily a benign disorder;Blood;2003-02-01
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