Clinical phenotype of haemoglobin Q-H disease
Author:
Publisher
BMJ
Subject
General Medicine,Pathology and Forensic Medicine
Cited by 20 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Hemoglobin profile and molecular characteristics of the complex interaction of hemoglobin Doi-Saket [α9(A7) asn > lys, HBA2:c.30C > a], a novel α2α1 hybrid globin variant, with hemoglobin E [β26(B8) Glu > lys, HBB:c.79G > A] and deletional α + -thalassemia in a Thai family;Annals of Medicine;2023-10-05
2. Haemoglobin analysis of a newborn with haemoglobin Q-H disease;Pathology;2023-04
3. 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
4. Telomere shortening correlates with disease severity in hemoglobin H disease patients;Blood Cells, Molecules, and Diseases;2021-07
5. Association of Hb A2 Variants with Several Forms of α- and β-Thalassemia in Thailand;Hemoglobin;2020-05-03
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