Article
Mapping of microsatellite markers in the Alagille region and screening of microdeletions by genotyping 23 patients.
European journal of human genetics : EJHG - 1 Jan 1994
Deleuze J F, Hazan J, Dhorne S, Weissenbach J, Hadchouel M
Abstract excerpt
Alagille syndrome (AGS) has been assigned to 20p11.23-20p12.2 according to minimum overlap between deletions observed on the chromosome 20 short arm of 9 patients. We report here the localisation of 5 microsatellite markers (D20S41, D20S48, D20S50, D20S56, and D20S58) within the deletion of one A...
Topics
- Alagille Syndrome
- Chromosome Mapping
- Chromosomes, Human, Pair 20
- DNA, Satellite
- Female
- Gene Deletion
- Genetic Markers
- Genotype
- Humans
- Male
- Pedigree
