ArticleJournal of medical genetics1992
Screening of microdeletions of chromosome 20 in patients with Alagille syndrome.
Article in Journal of medical genetics, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed.
- Human hepatic organoids for the analysis of human genetic diseases.JCI insight · 2017Article
- [Endocrinologic and metabolic complications of Alagille syndrome].Medizinische Klinik (Munich, Germany : 1983) · 1997Article
- Alagille syndrome.Journal of medical genetics · 1997Review
- Extinction of peroxisomal functions in hepatoma cell-fibroblast hybrids.Biochemical genetics · 1996Article
- Paucity of intrahepatic bile ducts, solitary kidney and atrophic pancreas with diabetes mellitus: atypical Alagille syndrome?European journal of pediatrics · 1996Article
- Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation family.Human genetics · 1995Article
- Deleted chromosome 20 from a patient with Alagille syndrome isolated in a cell hybrid through leucine transport selection: study of three candidate genes.Mammalian genome : official journal of the International Mammalian Genome Society · 1994Article
- Cytologically balanced t(2;20) in a two-generation family with alagille syndrome: cytogenetic and molecular studies.American journal of human genetics · 1994Article
- Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridization.Human genetics · 1993Article
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Authors and funding
6 authors.
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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.
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