/manager/Index ${session.getAttribute("locale")} 5 Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients /manager/Repository/uon:14804 Wed 11 Apr 2018 14:46:12 AEST ]]> A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology /manager/Repository/uon:7144 Sat 24 Mar 2018 08:34:14 AEDT ]]>