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JAGGED1 expression in human embryos: correlation with the Alagille syndrome phenotype
Alagille syndrome (AGS, MIM 118450) is an autosomal dominant disorder with a variable phenotype characterised by hepatic, eye, cardiac, and skeletal malformations and a characteristic facial appearance. Mutations within the gene JAGGED1 (JAG1), which encodes a ligand for NOTCH receptor(s), has been...
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| Main Authors: | , , |
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| Format: | Artigo |
| Language: | Inglês |
| Published: |
BMJ Group
2000
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1734694/ https://ncbi.nlm.nih.gov/pubmed/10978356 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.37.9.658 |
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