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Unique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypes.
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- European Journal of Human Genetics, 2012, v. 20, n. 3, p. 283, doi. 10.1038/ejhg.2011.187
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- Article
A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes.
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- Nature Genetics, 2009, v. 41, n. 12, p. 1269, doi. 10.1038/ng.481
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- Article