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Article

Novel intronic JAG1 variant associated with Alagille syndrome in a three-generation Lebanese family with variable features.

Clinical dysmorphology - 1 Apr 2023

Awwad Johnny, Yammine Tony, Hamdar Layal, Souaid Mirna, Farra Chantal

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PMID: 36779797
DOI: 10.1097/MCD.0000000000000447

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Novel intronic JAG1 variant associated with Alagille syndrome in a three-generation Lebanese family with variable features.PMID 36779797Read ↗

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Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.Semantic proximity Read ↗

Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.Semantic proximity Read ↗

Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.Semantic proximity Read ↗

Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.Semantic proximity Read ↗

Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.Semantic proximity Read ↗

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