Screening of microdeletions of chromosome 20 in patients with Alagille syndrome.
case_series · Level IV
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- Record sourced from PubMed, PMID 1583641.
- Also identified by PMC identifier 1015919.
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Abstract
We report a cytogenetic and molecular study of a series of patients with Alagille syndrome. All 14 patients were studied with high resolution banding techniques and eight of them were also analysed with non-radioactive in situ hybridisation of the cosmid probe D20S6. Seven of these eight patients were also studied for allelic losses at the D20S6 locus. No microdeletion of chromosome 20 was found in this series.
Medical subject headings
- Alagille Syndrome
- Chromosome Deletion
- Chromosomes, Human, Pair 20