Genetic diagnosis of haemophilia A of Chinese origin
- 1 November 1995
- journal article
- Published by Wiley in British Journal of Haematology
- Vol. 91 (3) , 722-727
- https://doi.org/10.1111/j.1365-2141.1995.tb05375.x
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Analysis of intron 22 inversions of the factor VIII gene in severe hemophilia A: implications for genetic counselingBlood, 1994
- Inversions disrupting the factor VIII gene are a common cause of severe haemophilia ANature Genetics, 1993
- Current methods of mutation detectionMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1993
- Molecular characterization of mild-to-moderate hemophilia A: detection of the mutation in 25 of 29 patients by denaturing gradient gel electrophoresis.Proceedings of the National Academy of Sciences, 1991
- Molecular characterization of severe hemophilia A suggests that about half the mutations are not within the coding regions and splice junctions of the factor VIII gene.Proceedings of the National Academy of Sciences, 1991
- Haemophilia A diagnosis by analysis of a hypervariable dinucleotide repeat within the factor VIII geneThe Lancet, 1991
- GENETIC PREDICTION OF HEMOPHILIA APublished by Elsevier ,1990
- Multiple Xbal polymorphisms for carrier detection and prenatal diagnosis of haemophilia ABritish Journal of Haematology, 1989
- An Improved Method for Prenatal Diagnosis of Genetic Diseases by Analysis of Amplified DNA SequencesNew England Journal of Medicine, 1987
- Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII geneNature, 1985