An Evaluation for the Causes of Reduced Hb A2 and the Molecular Characterization of HBD Variants in Hong Kong

Author:

Chan Nelson C. N.1ORCID,Wong Terry H. Y.2,Cheng Kelvin C. K.2,Chan Natalie P. H.2,Ng Margaret H. L.3

Affiliation:

1. Department of Pathology, Hong Kong Children’s Hospital, Kowloon Bay, Hong Kong

2. Department of Anatomical and Cellular Pathology, Prince of Wales Hospital, Shatin, New Territories, Hong Kong

3. Hematology, Genetics and Genomics Laboratory, Prince of Wales Hospital, Shatin, New Territories, affiliated to The Chinese University of Hong Kong, Hong Kong

Funder

Chinese Thalassemia Foundation

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Reference26 articles.

1. Antenatal screening for haemoglobinopathies: current status, barriers and ethics

2. Genomic evidence for independent origins of  -like globin genes in monotremes and therian mammals

3. HbA2: biology, clinical relevance and a possible target for ameliorating sickle cell disease

4. Prevalence and Genotypes of α- and β-Thalassemia Carriers in Hong Kong — Implications for Population Screening

5. Hong Kong College of Obstetricians and Gynaecologists. Guidelines of antenatal thalassaemia screening: the Hong Kong College of obstetricians and gynaecologists; 2003. Available from: https://www.who.int/genomics/elsi/regulatory_data/region/international/164/en/.

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