Alagille syndrome with de novo del(20) (p11.2)
- PMID: 1308363
- DOI: 10.1002/ajmg.1320420109
Alagille syndrome with de novo del(20) (p11.2)
Abstract
We report on an Arab boy with Alagille syndrome and a de novo deletion of the short arm of chromosome 20 with a 46,XY, del(20)(p11.2) chromosome constitution. Other reported cases are briefly reviewed.
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