Fetal Anemia and Hydrops Fetalis Associated with Homozygous Hb Constant Spring (HBA2: c.427T > C)
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269.2015.1126721
Reference20 articles.
1. Investigation and Management of Non-immune Fetal Hydrops
2. Nonimmune Hydrops Fetalis Diagnosed during the Second Half of Pregnancy in Southern China
3. Prenatal control of Hb Bart’s hydrops fetalis: a two-year experience at a mainland Chinese hospital
4. Hemoglobin H hydrops fetalis syndrome resulting from the association of the - -SEA deletion and the alphaQuong Szealpha mutation in a Chinese woman
5. Fetal anemia and hydrops associated with homozygosity for hemoglobin Quong Sze
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1. Routine antenatal molecular testing for α-thalassemia at a tertiary referral hospital in China: ten years of experience;Frontiers in Genetics;2024-06-04
2. Effective screening of hemoglobin Constant Spring and hemoglobin Paksé with several forms of α- and β-thalassemia in an area with a high prevalence and heterogeneity of thalassemia using capillary electrophoresis;Heliyon;2023-08
3. The Clinical Phenotypes of Alpha Thalassemia;Hematology/Oncology Clinics of North America;2023-04
4. Fetal Hemoglobin H Hydrops Fetalis: Another Three Case Reports;Hemoglobin;2023-03-04
5. Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden (HBA2:c.178G>C) and Hb Quong Sze (HBA2:c.377T>C);Journal of International Medical Research;2021-07
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