<?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%">Schulpis, K.H.</style></author><author><style face="normal" font="default" size="100%">Thodi, G.</style></author><author><style face="normal" font="default" size="100%">Chatzidaki, M.</style></author><author><style face="normal" font="default" size="100%">Iakovou, K.</style></author><author><style face="normal" font="default" size="100%">Molou, E.</style></author><author><style face="normal" font="default" size="100%">Dotsikas, Y.</style></author><author><style face="normal" font="default" size="100%">Loukas, Y.L.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Rare cases of galactose metabolic disorders: Identification of more than two mutations per patient</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Pediatric Endocrinology and Metabolism</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2017</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.scopus.com/inward/record.uri?eid=2-s2.0-85031041758&amp;doi=10.1515%2fjpem-2017-0263&amp;partnerID=40&amp;md5=ec5fbec5614a69740a88c0e923c3093f</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">10</style></number><volume><style face="normal" font="default" size="100%">30</style></volume><pages><style face="normal" font="default" size="100%">1119-1120</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><notes><style face="normal" font="default" size="100%">cited By 0</style></notes></record></records></xml>