Prenatal diagnosis of alpha and beta thalassemias and hemophilia A: experience in Hong Kong
- 1 February 1990
- journal article
- Published by Elsevier in Clinical Biochemistry
- Vol. 23 (1) , 79-84
- https://doi.org/10.1016/0009-9120(90)90525-y
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Different Forms of Hb H Disease in the ChineseHemoglobin, 1988
- Detection of sickle cell anaemia and thalassaemiasNature, 1987
- Organization of the ζ‐α genes in ChineseBritish Journal of Haematology, 1986
- Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell AnemiaScience, 1985
- Hydrops fetalis due to an unusual form of Hb H diseaseBlood, 1985
- A SIMPLE SENSITIVE PRENATAL TEST FOR HYDROPS FETALIS CAUSED BY α-THALASSAEMIAThe Lancet, 1984
- Prenatal diagnosis of homozygous alpha thalassaemia by direct DNA analysis of uncultured amniotic fluid cells.BMJ, 1984
- FIRST-TRIMESTER FETAL DIAGNOSIS FOR HAEMOGLOBINOPATHIES: THREE CASESThe Lancet, 1982
- Alpha‐Thalassaemia in Chinese: Cord Blood StudiesBritish Journal of Haematology, 1969
- Studies on haemoglobin Bart's (Hb??4) in Thailand: the incidence and the mechanism of occurrence in cord blood*Annals of Human Genetics, 1967