Detailed molecular and clinical characterization of three patients with 21q deletions.

Abstract

We have investigated three patients with 21q deletions, two with developmental delay, dysmorphic features and internal organ malformations, and one with cognitive function within the normal range but with some deficits in gross and fine motor development. All aberrations were characterized by array-comparative genomic hybridization (array-CGH). In addition… (More)
DOI: 10.1111/j.1399-0004.2009.01289.x

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