A case of transfusion-dependent nondeletional Hb H disease undiagnosed during prenatal screening for thalassemia
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference9 articles.
1. A laboratory strategy for genotyping haemoglobin H disease in the Chinese
2. Rapid molecular characterization of Hb H disease in Chinese by polymerase chain reaction
3. Genetic and Clinical Features of Hemoglobin H Disease in Chinese Patients
4. The interaction of α thalassaemia with heterozygous β thalassaemia
5. The distribution of the Hb Constant Spring gene in Southeast Asian populations
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1. A New Hemoglobin Variant: Hb Jiujiang [α18(A16)Gly→Cys, HBA2: c.55G>T];Hemoglobin;2021-07-04
2. Pre Gestational Thalassemia Screening in Mainland China: The First Two Years of a Preventive Program;Hemoglobin;2017-11-02
3. First Case of a Compound Heterozygosity for Two Nondeletionalα-Thalassemia mutations, Hb Constant Spring and Hb Quong Sze;Hemoglobin;2016-03-09
4. Identification of Nondeletionalα-Thalassemia in a Prenatal Screening Program by Reverse Dot-Blot in Southern China;Hemoglobin;2014-12-19
5. Co-inheritance of α-thalassaemia and β-thalassaemia in a prenatal screening population in mainland China;Journal of Medical Screening;2014-08-12
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