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Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome.

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Title: Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome.
Authors: Willemsen, Marjolein H.1 m.willemsen@antrg.umcn.nl, Fernandez, Bridget A.2, Bacino, Carlos A.3, Gerkes, Erica4, de Brouwer, Arjan P. M.1, Pfundt, Rolph1, Sikkema-Raddatz, Birgit4, Scherer, Stephen W.5, Marshall, Christian R.5, Potocki, Lorraine3, van Bokhoven, Hans1, Kleefstra, Tjitske1
Source: European Journal of Human Genetics. Apr2010, Vol. 18 Issue 4, p429-435. 7p. 1 Black and White Photograph, 1 Diagram, 2 Charts.
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  Data: Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome.
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  Data: <searchLink fieldCode="JN" term="%22European+Journal+of+Human+Genetics%22">European Journal of Human Genetics</searchLink>. Apr2010, Vol. 18 Issue 4, p429-435. 7p. 1 Black and White Photograph, 1 Diagram, 2 Charts.
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        Value: 10.1038/ejhg.2009.192
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              Text: Apr2010
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