<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Korenberg, J. R.</style></author><author><style face="normal" font="default" size="100%">Dai, L.</style></author><author><style face="normal" font="default" size="100%">Bellugi, U.</style></author><author><style face="normal" font="default" size="100%">Jarvinen-Pasley, A.</style></author><author><style face="normal" font="default" size="100%">Mills, D.</style></author><author><style face="normal" font="default" size="100%">Galaburda, A.</style></author><author><style face="normal" font="default" size="100%">Reiss, A.</style></author><author><style face="normal" font="default" size="100%">Pober, B. R.</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Epstein, Charles J.</style></author><author><style face="normal" font="default" size="100%">Erickson, Robert P.</style></author><author><style face="normal" font="default" size="100%">Wynshaw-Boris, Anthony Joseph</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Deletion of 7q11.23 Genes and Williams Syndrome</style></title><secondary-title><style face="normal" font="default" size="100%">Inborn errors of development : the molecular basis of clinical disorders of morphogenesis</style></secondary-title><tertiary-title><style face="normal" font="default" size="100%">Oxford monographs on medical genetics</style></tertiary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Congenital Abnormalities genetics.</style></keyword><keyword><style  face="normal" font="default" size="100%">Developmental disabilities Genetic aspects.</style></keyword><keyword><style  face="normal" font="default" size="100%">Developmental genetics.</style></keyword><keyword><style  face="normal" font="default" size="100%">Genetic Diseases</style></keyword><keyword><style  face="normal" font="default" size="100%">Genetic disorders in children.</style></keyword><keyword><style  face="normal" font="default" size="100%">Genetic disorders.</style></keyword><keyword><style  face="normal" font="default" size="100%">Human Development.</style></keyword><keyword><style  face="normal" font="default" size="100%">Inborn genetics.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://lccn.loc.gov/2007027492</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">54</style></number><edition><style face="normal" font="default" size="100%">2nd</style></edition><publisher><style face="normal" font="default" size="100%">Oxford University Press</style></publisher><pub-location><style face="normal" font="default" size="100%">Oxford ; New York</style></pub-location><pages><style face="normal" font="default" size="100%">1617 p.</style></pages><isbn><style face="normal" font="default" size="100%">9780195306910 </style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><notes><style face="normal" font="default" size="100%">&lt;p&gt;edited by Charles J. Epstein, Robert P. Erickson, Anthony Wynshaw-Boris.&lt;/p&gt;</style></notes></record></records></xml>