Deletion of 3p25.3 in a patient with intellectual disability and dysmorphic features with further definition of a critical region.

@article{Kellogg2013DeletionO3,
  title={Deletion of 3p25.3 in a patient with intellectual disability and dysmorphic features with further definition of a critical region.},
  author={Gregory Kellogg and John Sum and Robert Wallerstein},
  journal={American journal of medical genetics. Part A},
  year={2013},
  volume={161A 6},
  pages={1405-8}
}
Several recent reports of interstitial deletions at the terminal end of the short arm of chromosome 3 have helped to define the critical region whose deletion causes 3p deletion syndrome. We report on an 11-year-old girl with intellectual disability, obsessive-compulsive tendencies, hypotonia, and dysmorphic facial features in whom a 684 kb interstitial 3p25.3 deletion was characterized using array-CGH. This deletion overlaps with interstitial 3p25 deletions reported in three recent case… CONTINUE READING
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Molecular characterization and clinical features of a patient with an interstitial deletion of 3p25.3–p26.1

  • C Gunnarsson, C. Foyn Bruun
  • Am J Med Genet Part A 152A:3110–3114
  • 2010
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