Hemoglobin Q-Thailand related disorders: Origin, molecular, hematological and diagnostic aspects
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference23 articles.
1. Hemoglobinopathies in Southeast Asia;Fucharoen;Hemoglobin,1987
2. Hb Q-Thailand [α 74(EF3)Asp➔His]: gene organization, molecular structure, and DNA diagnosis;Zeng;Hemoglobin,1992
3. Hb Q-Thailand-Hb H disease in a Chinese living in Geneva, Switzerland: characterization of the variant and identification of the two α-thalassemic chromosomes;Beris;Am. J. Hematol.,1987
4. Clinical phenotype of haemoglobin Q-H disease;Leung;J. Clin. Pathol.,2004
5. Four cases of Hb Q-H disease found in Southern China;Li;Hemoglobin,2007
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1. A large cohort of Hb H disease in northeast Thailand: A molecular revisited, diverse genetic interactions and identification of a novel mutation;Clinica Chimica Acta;2024-07
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4. Hb Q-Thailand heterozygosity unlinked with the (–α 4.2 /) α + -thalassemia deletion allele identified by long-read SMRT sequencing: hematological and molecular analyses;Hematology;2023-03-03
5. Molecular epidemiological investigation of abnormal hemoglobin in Shaokwan region, southern China;Hematology;2022-01-24
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