Total: 1 |
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PMID (PMCID) | ||
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18627067 |
MALE | Child |
Homozygous deletions of a copy number change detected by array CGH: a new cause for mental retardation? | ||
Curry CJ, Mao R, Aston E, Mongia SK, Treisman T, Procter M, Chou B, Whitby H, South ST, Brothman AR. Am J Med Genet A. 2008;146A(15):1903-10. |
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This patient has mild craniofacial dysmorphic features, bifid uvula, peripheral pulmonic stenosis and developmental delay. |