<?xml version='1.0' encoding='UTF-8'?><xml><records><record><source-app name="HighWire" version="7.x">Drupal-HighWire</source-app><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lederman, Lynne</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Vandenberghe, Peter</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Noninvasive Detection of Genomic Imbalances in HL Is Promising</style></title><secondary-title><style face="normal" font="default" size="100%">MD Conference Express</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2014-12-01 00:00:00</style></date></pub-dates></dates><pages><style  face="normal" font="default" size="100%">18-19</style></pages><abstract><style  face="normal" font="default" size="100%">Noninvasive massive parallel sequencing of circulating cell-free DNA allows the identification of genomic imbalances in Hodgkin/Reed-Sternberg cells in early and advanced stage NSHL. This discovery may facilitate the development of predictive biomarkers and monitoring early disease response to therapy. These issues will be investigated in the context of clinical trials.</style></abstract><number><style face="normal" font="default" size="100%">55</style></number><volume><style face="normal" font="default" size="100%">14</style></volume></record></records></xml>