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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 AGS patient. This study allows an estimation of the genetic extent of this deletion as being between 30 and 36 cM, and...

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PMID: 7834278
DOI: 10.1159/000472362

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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