3 Prenatal diagnosis of haemophilia
- 1 June 1996
- journal article
- review article
- Published by Elsevier in Bailliere's Clinical Haematology
- Vol. 9 (2), 243-257
- https://doi.org/10.1016/s0950-3536(96)80061-8
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- The impact of prenatal diagnosis on the incidence of haemophilia in SwedenHaemophilia, 1995
- Inversions disrupting the factor VIII gene are a common cause of severe haemophilia ANature Genetics, 1993
- Characteristic mRNA abnormality found in half the patients with severe haemophilia A is due to large DNA inversionsHuman Molecular Genetics, 1993
- Origin of mutation in sporadic cases of haemophilia‐BEuropean Journal of Haematology, 1992
- More Than Half the Sporadic Cases of Hemophilia A in Sweden Are Due to a Recent MutationActa Paediatrica, 1991
- How Do Carriers of Hemophilia Experience Prenatal Diagnosis (PND)?Carriers’Immediate and Later Reactions to Amniocentesis and Fetal Blood SamplingActa Paediatrica, 1989
- Characterization of the human factor VIII geneNature, 1984
- PLASMA ASSAY OF FETAL FACTORS VIIIC AND IX FOR PRENATAL DIAGNOSIS OF HÆMOPHILIAThe Lancet, 1979
- Sampling pure fetal blood by fetoscopy in second trimester of pregnancy.BMJ, 1978
- Detection of specific sequences among DNA fragments separated by gel electrophoresisJournal of Molecular Biology, 1975