Prenatal Diagnosis of α- and β-Thalassemias: Experience in Hong Kong
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630268808991671
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4. Gene deletion as the cause of α thalassaemia: Genetic lesion in homozygous α thalassaemia (hydrops fetalis)
5. Diagnosis of Homozygous α-Thalassemia in Cultured Amniotic-Fluid Fibroblasts
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1. Outcomes and morbidities of patients who survive haemoglobin Bart’s hydrops fetalis syndrome: 20-year retrospective review;Hong Kong Medical Journal;2018-04-06
2. Recommendations for introducing genetics services in developing countries;Nature Reviews Genetics;2003-01
3. Ten Years' Experience of Antenatal Mean Corpuscular Volume Screening and Prenatal Diagnosis for Thalassaemias in Hong Kong;Journal of Obstetrics and Gynaecology Research;2000-06
4. Prevention of β-Thalassemia Major by Antenatal Screening in Hong Kong;Pediatric Hematology and Oncology;1998-01
5. α Thalassemia;Hemoglobin;1989-01
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