Prenatal diagnosis of alpha and beta thalassemias and hemophilia A: experience in Hong Kong
Author:
Publisher
Elsevier BV
Subject
Clinical Biochemistry,General Medicine
Reference33 articles.
1. Alpha-thalassemia in Chinese: cord blood studies;todd;Br J Haemat,1969
2. Studies on haemoglobin Bart's (Hb-gamma4) in Thailand: the incidence and the mechanism of occurrence in cord blood;Pootrakul;Ann Hum Genet,1967
3. Homozygous alpha thalassemia: clinical presentation, diagnosis and management;Liang;Br J Obstet Gynaecol,1985
4. Prenatal diagnosis of homozygous alpha thalassemia by direct DNA analysis of uncultured amniotic cells;Chan;Br Med J,1984
5. First-trimester fetal diagnosis for haemoglobinopathies: three cases;Old;Lancet,1982
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1. Clinical and molecular characteristics of hemophilia A affected individuals and carriers: A 24 years experience from three centers;American Journal of Medical Genetics Part A;2024-05-15
2. Comparison of the HbH inclusion test and a PCR test in routine screening for alpha thalassaemia in Hong Kong.;Journal of Clinical Pathology;1996-05-01
3. Prenatal screening for haemoglobin disorders;Prenatal Diagnosis;1995-12
4. DNA diagnosis for the detection of sickle hemoglobinopathies;American Journal of Hematology;1993-06
5. 5 Antenatal diagnosis;Baillière's Clinical Haematology;1991-04
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