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