Article
Multiplex analysis of two intragenic microsatellite repeat polymorphisms in the genetic diagnosis of haemophilia A.
British journal of haematology - 1 Apr 1994
Windsor S, Taylor S A, Lillicrap D
Abstract excerpt
Use of molecular genetic studies for carrier detection and prenatal diagnosis of haemophilia A will be informative in approximately 75% of kindreds with a prior history of the disorder if previously reported bi-allelic intragenic polymorphisms are used. In this study we report the use of two mult...
Topics
- Alleles
- Base Sequence
- Case-Control Studies
- DNA, Satellite
- Factor VIII
- Female
- Fetal Diseases
- Genetic Carrier Screening
- Hemophilia A
- Humans
- Introns
- Male
- Molecular Sequence Data