First Case of a Compound Heterozygosity for Two Nondeletionalα-Thalassemia mutations, Hb Constant Spring and Hb Quong Sze
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269.2016.1148614
Reference13 articles.
1. The distribution of the Hb Constant Spring gene in Southeast Asian populations
2. Detection of the HB Quong SZE Mutation in a Chinese Family by Selective Amplification of the α2-Globin Gene and Restriction Map Analysis with MSP I
3. Fetal anemia and hydrops associated with homozygosity for hemoglobin Quong Sze
4. Anemia and Hydrops in a Fetus With Homozygous Hemoglobin Constant Spring
5. Genetic and Clinical Features of Hemoglobin H Disease in Chinese Patients
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1. Non-deletional haemoglobin H (Hb H) disease morphologically masquerading as congenital dyserythropoietic anaemia type II: a diagnostic pitfall;Journal of Clinical Pathology;2023-12-20
2. Identification of Two Novel Thalassemia Variants, HBA1: c.263delA and HBA2: c.376dupC, in Chinese Individuals;Hemoglobin;2021-01-02
3. A Novel α-Thalassemia Nonsense Mutation on the α2-Globin Gene: HBA2: c.184A>T;Hemoglobin;2017-11-02
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