Screening and Diagnosis of Hb Quong Sze [HBA2: c.377T > C (orHBA1)] in a Prenatal Control Program for Thalassemia
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269.2014.910669
Reference15 articles.
1. Globin structural mutant α125Leu→Pro is a novel cause of α-thalassaemia
2. Detection of the HB Quong SZE Mutation in a Chinese Family by Selective Amplification of the α2-Globin Gene and Restriction Map Analysis with MSP I
3. Fetal anemia and hydrops associated with homozygosity for hemoglobin Quong Sze
4. Hemoglobin H hydrops fetalis syndrome resulting from the association of the - -SEA deletion and the alphaQuong Szealpha mutation in a Chinese woman
5. A Reliable Screening Protocol for Thalassemia and Hemoglobinopathies in Pregnancy
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1. Molecular analysis and clinical significance of hemoglobin Quong Sze in Huizhou city, Southern China;Taiwanese Journal of Obstetrics and Gynecology;2023-09
2. Clinical and Haematological Parameters of Commonly Reported Non-deletional α-thalassaemia Mutations in Southeast Asia: A Review;Malaysian Journal of Medicine and Health Sciences;2022-09-15
3. Combined Gap-Polymerase Chain Reaction and Targeted Next-Generation Sequencing Improve α- and β-Thalassemia Carrier Screening in Pregnant Women in Vietnam;Hemoglobin;2022-07-04
4. Genetic counseling and prenatal decision for hemoglobin H disease caused by the rare α2 codon 30 (-GAG) (HBA2: c.91_93delGAG) mutation and the SEA deletion: Case series study;Taiwanese Journal of Obstetrics and Gynecology;2021-07
5. Cell count‐based parameters and algorithms for thalassaemia trait screening in the southern Chinese population;International Journal of Laboratory Hematology;2021-01-06
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