Phenotypic Variability in a Chinese Family with Nondeletional Hb H-Hb Quong Sze Disease
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269.2011.592554
Reference6 articles.
1. Hemoglobin H disease: not necessarily a benign disorder
2. Clinical and molecular analysis of haemoglobin H disease in Sardinia: haematological, obstetric and cardiac aspects in patients with different genotypes
3. A Severe α Thalassemia Case Compound Heterozygous for Hb Adana in α1 Gene and 20.5 kb Double Gene Deletion
4. Diversity in clinical presentation of hemoglobin H disease induced by the SEA deletion and the hemoglobin Quong Sze
5. Detection of Hb Constant Spring by a Capillary Electrophoresis Method
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2. Genetic counseling and prenatal decision for hemoglobin H disease caused by the rare α2 codon 30 (-GAG) (HBA2: c.91_93delGAG) mutation and the SEA deletion: Case series study;Taiwanese Journal of Obstetrics and Gynecology;2021-07
3. First Report of Nondeletional Hb H Disease Caused by an α2-Globin Gene Mutation: HBA2: c.184A>T;Hemoglobin;2021-05-04
4. First Report of a Case with Nondeletional Hb H Disease Caused by IVS-I-116 (A>G) of the α2-Globin Gene;Hemoglobin;2018-11-02
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