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.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/ajmg.1320420109 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!