Erratum to: An Interstitial 15q11–q14 Deletion: Expanded Prader–Willi Syndrome Phenotype (DOI 10.1002/ajmg.a.33197; Am J Med Genet Part A 152A:404–408)

Authors

  • Merlin G. Butler,

  • Douglas C. Bittel,

  • Nataliya Kibiryeva,

  • Linda D. Cooley,

  • Shihui Yu

Errata

This article corrects:


    • How to cite this article: Butler MG, Bittel DC, Kibiryeva N, Cooley LD, Yu S. 2010. Erratum to: An interstitial 15q11–q14 deletion: Expanded Prader–Willi syndrome phenotype (DOI 10.1002/ajmg.a33197; Am J Med Genet Part A 152A: 404–408). Am J Med Genet Part A 152A:1331–1332.

    In publishing the figures for this manuscript, captions from another submission were inadvertently associated with and printed under Figures 2 and 3.

    Figure 2.

    Frontal views taken at 8, 14, and 21 months of age showing typical facial features of Prader-Willi syndrome. [Color figure can be viewed in the online issue, which is available at www.interscience.wiley.com.]

    Figure 3.

    Array comparative genomic hybridization (aCGH) comparing our subject with the 15q11-q14 deletion to chromosomally normal DNA. Upper panel shows an expansion of the deleted region with the location of the breakpoints and the genes within the region. [Color figure can be viewed in the online issue, which is available at www.interscience.wiley.com.]

    The Publisher sincerely regrets the error. The figure legends should have read:

    Ancillary