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Published on: February 18, 2013
11p15.4 Microdeletion Associates with Hemihypertrophy
Surasak Puvabanditsin1, Mehrin Sadiq1, Marianne Jacob1
1Department of Pediatrics, Rutgers Robert Wood Johnson Medical School, New Brunswick, NJ, USA.
Abstract:
We report a preterm female infant with intrauterine growth retardation, dysmorphic facies, missing rib, small hands and feet, and hemihypertrophy. The results of whole genome SNP microarray analysis showed approximately 77 Kb interstitial deletion of the short arm of chromosome 11 (11p15.4). We report novel clinical findings of this rare genetic condition.
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