Prenatal diagnosis of haemoglobin disorders by cordocentesis at 12 weeks' gestation
- 1 December 1991
- journal article
- research article
- Published by Wiley in Prenatal Diagnosis
- Vol. 11 (12) , 899-904
- https://doi.org/10.1002/pd.1970111204
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- The risks of early cordocentesis (12–21 weeks): Analysis of 500 proceduresPrenatal Diagnosis, 1990
- The Safety and Efficacy of Chorionic Villus Sampling for Early Prenatal Diagnosis of Cytogenetic AbnormalitiesNew England Journal of Medicine, 1989
- Molecular basis and prenatal diagnosis of beta-thalassemiaBlood, 1988
- The spectrum of β-thalassaemia mutations in SicilyBritish Journal of Haematology, 1988
- A simple approach to prenatal diagnosis of beta-thalassemia in a geographic area where multiple mutations occurBlood, 1988
- Measurement of human fetoplacental blood volume in erythroblastosis fetalisAmerican Journal of Obstetrics and Gynecology, 1987
- βA and βthal DNA haplotypes in SicilyHuman Genetics, 1986
- Advances in the prenatal diagnosis of hematologic diseasesBlood, 1984
- Prenatal diagnosis of hemoglobinopathies: comparison of the results obtained by isoelectric focusing of hemoglobins and by chromatography of radioactive globin chainsBlood, 1980
- A standard of fetal growth for the united states of AmericaAmerican Journal of Obstetrics and Gynecology, 1976