Invasive prenatal diagnosis of α-thalassemia to control Hb Bart’s hydrops fetalis syndrome: 15 years of experience
Author:
Publisher
Springer Science and Business Media LLC
Subject
Obstetrics and Gynecology,General Medicine
Link
http://link.springer.com/article/10.1007/s00404-018-4807-4/fulltext.html
Reference24 articles.
1. Higgs DR, Vickers MA, Wilkie AO, Pretorius IM, Jarman AP, Weatherall DJ (1989) A review of the molecular genetics of the human alpha-globin gene cluster. Blood 73(5):1081–1104
2. Farashi S, Harteveld CL (2017) Molecular basis of alpha-thalassemia. Blood Cells Mol Dis. https://doi.org/10.1016/j.bcmd.2017.09.004
3. Weatherall DJ, Clegg JB (2001) Inherited haemoglobin disorders: an increasing global health problem. Bull World Health Organ 79(8):704–712
4. Harteveld CL, Higgs DR (2010) Alpha-thalassaemia. Orphanet J Rare Dis 5:13. https://doi.org/10.1186/1750-1172-5-13
5. Weatherall DJ (1980) The thalassemia syndromes. Tex Rep Biol Med 40:323–333
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1. Appropriate whole genome amplification and pathogenic loci detection can improve the accuracy of preimplantation genetic diagnosis for deletional α-thalassemia;Frontiers in Endocrinology;2024-03-08
2. Ten years’ experience in prenatal diagnosis of α-thalassemia in a municipal hospital and retrospective analysis of ultrasonic abnormalities;International Journal of Hematology;2023-07-21
3. A novel 15.8 kb deletion α-thalassemia confirmed by long-read single-molecule real-time sequencing: Hematological phenotypes and molecular characterization;Clinical Biochemistry;2022-10
4. Erythroblastosis Fetalis, Hydrops Fetalis, and Transplacental Hemorrhage;Benirschke's Pathology of the Human Placenta;2021-12-08
5. Pregnancy outcomes in women affected by fetal alpha-thalassemia: a case control study;Scientific Reports;2021-08-27
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