<?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%">Sismani, C</style></author><author><style face="normal" font="default" size="100%">Donoghue, J</style></author><author><style face="normal" font="default" size="100%">Alexandrou, A</style></author><author><style face="normal" font="default" size="100%">Karkaletsi, M</style></author><author><style face="normal" font="default" size="100%">Christopoulou, S</style></author><author><style face="normal" font="default" size="100%">Konstantinidou, AE</style></author><author><style face="normal" font="default" size="100%">Livanos, P</style></author><author><style face="normal" font="default" size="100%">Patsalis, PC</style></author><author><style face="normal" font="default" size="100%">Velissariou, V</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A prenatally ascertained, maternally inherited 14.8 Mb duplication of chromosomal bands Xq13. 2–q21. 31 associated with multiple congenital abnormalities in a male fetus</style></title><secondary-title><style face="normal" font="default" size="100%">Gene</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2013</style></year></dates><publisher><style face="normal" font="default" size="100%">Elsevier</style></publisher><volume><style face="normal" font="default" size="100%">530</style></volume><pages><style face="normal" font="default" size="100%">138-142</style></pages><isbn><style face="normal" font="default" size="100%">0378-1119</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><issue><style face="normal" font="default" size="100%">1</style></issue></record></records></xml>