Interstitial deletion of chromosome 18[del(18)(q11.2q12.2 or q12.2q21.1]

Abstract
A 27-month-old boy with mild developmental delay, growth delay, strabismus, midface hypoplasia, relative telecanthus, downslanting palpebral fissures, epicanthal folds, dental hypoplasia, and cardiac defects was found to have an interstitial deletion of chromosome 18 involving band q12.1 or q12.3.

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