Hydrops Fetalis Associated with Homozygosity for Hb Adana [α59(E8)Gly→Asp (α2)]
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269.2010.493405
Reference21 articles.
1. Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care Problem
2. Alpha-chain Thalassemia and Hydrops Fetalis in Malaya: Report of Five Cases
3. Hydrops Foetalis with a Fast-moving Haemoglobin
4. Hb adana or α259(E8)Gly→Aspβ2, A severely unstable α1-globin variant, observed in combination with the -(α)20.5 KB α-thal-1 deletion in two Turkish patients
5. Interaction of an α+-Thalassemia Deletion with Either a Highly Unstable α-Globin Variant (α2, Codon 59, GGC→GAC) or a Nondeletional α-Thalassemia Mutation (AATAA→AATAAG): Comparison of Phenotypes Illustrating “Dominant” α-Thalassemia
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2. Genetic heterogeneity of thalassemia major patients in Rembang Regency, Central Java, Indonesia;Bali Medical Journal;2023-05-18
3. 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
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