De novo interstitial deletion of 3q22.3-q25.2 encompassing FOXL2, ATR, ZIC1, and ZIC4 in a patient with blepharophimosis/ptosis/epicanthus inversus syndrome, Dandy-Walker malformation, and global developmental delay.

Source:http://linkedlifedata.com/resource/pubmed/id/21471554

Download in:

View as

General Info

PMID
21471554