Fetal Hemoglobin H Hydrops Fetalis: Another Three Case Reports
Author:
Affiliation:
1. Prenatal Diagnosis Unit, Boai Hospital of Zhongshan, Zhongshan, Guangdong, People’s Republic of China
2. Prenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center, Guangzhou, Guangdong, People’s Republic of China
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
https://www.tandfonline.com/doi/pdf/10.1080/03630269.2023.2215445
Reference21 articles.
1. The α-Thalassemias
2. Heterogeneity of Hemoglobin H Disease in Childhood
3. Clinical Features and Genotypes of Patients with Hemoglobin H Disease in Taiwan
4. Hb H Hydrops Fetalis Syndrome Caused by Association of the − −SEADeletion and Hb Constant Spring (HBA2: c.427T > C) Mutation in a Chinese Family
5. Hemoglobin H hydrops fetalis syndrome resulting from the association of the - -SEA deletion and the alphaQuong Szealpha mutation in a Chinese woman
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