<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mills, D.L.</style></author><author><style face="normal" font="default" size="100%">Dai, L.</style></author><author><style face="normal" font="default" size="100%">Yam, A.</style></author><author><style face="normal" font="default" size="100%">Fishman, I.</style></author><author><style face="normal" font="default" size="100%">Bellugi, U.</style></author><author><style face="normal" font="default" size="100%">Reiss, A.L.</style></author><author><style face="normal" font="default" size="100%">Korenberg, J.R.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Genetic mapping of brain plasticity in Williams Syndrome: ERP markers of face and language processing across development</style></title><secondary-title><style face="normal" font="default" size="100%">Dev Neuropsychol</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2013</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.ncbi.nlm.nih.gov/pubmed/24219698</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">38</style></volume><pages><style face="normal" font="default" size="100%">613-642</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;In&amp;nbsp;&lt;span class=&quot;highlight&quot; style=&quot;background-color: rgb(242, 245, 248); &quot;&gt;Williams&lt;/span&gt;&amp;nbsp;&lt;span class=&quot;highlight&quot; style=&quot;background-color: rgb(242, 245, 248); &quot;&gt;Syndrome&lt;/span&gt;&amp;nbsp;(WS), a known&amp;nbsp;&lt;span class=&quot;highlight&quot; style=&quot;background-color: rgb(242, 245, 248); &quot;&gt;genetic&lt;/span&gt;&amp;nbsp;deletion results in atypical&amp;nbsp;&lt;span class=&quot;highlight&quot; style=&quot;background-color: rgb(242, 245, 248); &quot;&gt;brain&lt;/span&gt;&amp;nbsp;function with strengths in&amp;nbsp;&lt;span class=&quot;highlight&quot; style=&quot;background-color: rgb(242, 245, 248); &quot;&gt;face&lt;/span&gt;&amp;nbsp;and&amp;nbsp;&lt;span class=&quot;highlight&quot; style=&quot;background-color: rgb(242, 245, 248); &quot;&gt;language&lt;/span&gt;&lt;span class=&quot;highlight&quot; style=&quot;background-color: rgb(242, 245, 248); &quot;&gt;processing&lt;/span&gt;. We examined how&amp;nbsp;&lt;span class=&quot;highlight&quot; style=&quot;background-color: rgb(242, 245, 248); &quot;&gt;genetic&lt;/span&gt;&amp;nbsp;influences on&amp;nbsp;&lt;span class=&quot;highlight&quot; style=&quot;background-color: rgb(242, 245, 248); &quot;&gt;brain&lt;/span&gt;&amp;nbsp;activity change with&amp;nbsp;&lt;span class=&quot;highlight&quot; style=&quot;background-color: rgb(242, 245, 248); &quot;&gt;development&lt;/span&gt;. In three studies, event-related potentials (ERPs) from large samples of children, adolescents, and adults with the full&amp;nbsp;&lt;span class=&quot;highlight&quot; style=&quot;background-color: rgb(242, 245, 248); &quot;&gt;genetic&lt;/span&gt;&amp;nbsp;deletion for WS were compared to typically developing controls, and two adults with partial deletions for WS. Studies 1 and 2 identified&amp;nbsp;&lt;span class=&quot;highlight&quot; style=&quot;background-color: rgb(242, 245, 248); &quot;&gt;ERP&lt;/span&gt;&amp;nbsp;&lt;span class=&quot;highlight&quot; style=&quot;background-color: rgb(242, 245, 248); &quot;&gt;markers&lt;/span&gt;&amp;nbsp;of&amp;nbsp;&lt;span class=&quot;highlight&quot; style=&quot;background-color: rgb(242, 245, 248); &quot;&gt;brain&lt;/span&gt;&lt;span class=&quot;highlight&quot; style=&quot;background-color: rgb(242, 245, 248); &quot;&gt;plasticity&lt;/span&gt;&amp;nbsp;in WS&amp;nbsp;&lt;span class=&quot;highlight&quot; style=&quot;background-color: rgb(242, 245, 248); &quot;&gt;across&lt;/span&gt;&amp;nbsp;&lt;span class=&quot;highlight&quot; style=&quot;background-color: rgb(242, 245, 248); &quot;&gt;development&lt;/span&gt;. Study 3 suggested that, in adults with partial deletions for WS, specific genes may be differentially implicated in&amp;nbsp;&lt;span class=&quot;highlight&quot; style=&quot;background-color: rgb(242, 245, 248); &quot;&gt;face&lt;/span&gt;&amp;nbsp;and&amp;nbsp;&lt;span class=&quot;highlight&quot; style=&quot;background-color: rgb(242, 245, 248); &quot;&gt;language&lt;/span&gt;&amp;nbsp;&lt;span class=&quot;highlight&quot; style=&quot;background-color: rgb(242, 245, 248); &quot;&gt;processing&lt;/span&gt;.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">8</style></issue><accession-num><style face="normal" font="default" size="100%">24219698</style></accession-num><custom2><style face="normal" font="default" size="100%">PMC3695384</style></custom2></record></records></xml>