Misdiagnosis of Hb Constant Spring (α142, Term→Gln,TAA→CAA in α2) in a Hb H (β4) Disease Child
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.1080/03630260601059332
Reference7 articles.
1. Genetic and Clinical Features of Hemoglobin H Disease in Chinese Patients
2. The distribution of the Hb Constant Spring gene in Southeast Asian populations
3. Rapid molecular characterization of Hb H disease in Chinese by polymerase chain reaction
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2. A New Hemoglobin Variant: Hb Jiujiang [α18(A16)Gly→Cys, HBA2: c.55G>T];Hemoglobin;2021-07-04
3. Non-deletional alpha thalassaemia: a review;Orphanet Journal of Rare Diseases;2020-06-29
4. Co-inheritance of α-thalassaemia and β-thalassaemia in a prenatal screening population in mainland China;Journal of Medical Screening;2014-08-12
5. Prevalence and Molecular Characterization of Structural Hemoglobin Variants in the Dongguan Region of Guangdong Province, Southern China;Hemoglobin;2014-07-02
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