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. 2016 Feb;8(2):a019497. doi: 10.1101/cshperspect.a019497

Figure 4.

Figure 4.

Images of a Prader–Willi syndrome patient (A) and Angelman syndrome patient (B) illustrate the dramatic differences in the clinical features of the disorders resulting from defects in an imprinted region. (Images kindly provided by Dr. Daniel J. Driscoll and Dr. Carlos A. Bacino, respectively.)