https://nova.newcastle.edu.au/vital/access/ /manager/Index ${session.getAttribute("locale")} 5 New EPCAM founder deletion in Polish population https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:34658 A in MLH1 gene and c.942+3A > T in MSH2, the deletion mutation encompassing EPCAM is one of the most common causative changes responsible for LS in Poland.]]> Wed 09 Feb 2022 15:54:51 AEDT ]]> Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:34524 Wed 06 Apr 2022 13:58:28 AEST ]]> Exome sequencing of familial adenomatous polyposis-like individuals identifies both known and novel causative genes https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:48845 Thu 20 Apr 2023 10:58:52 AEST ]]> Further delineation of dosage-sensitive K/L mediated Xq28 duplication syndrome includes incomplete penetrance https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:50870 Thu 17 Aug 2023 11:14:48 AEST ]]> Restoring reproductive confidence in families with X-linked mental retardation by finding the causal mutation (letter) https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:5656 Sat 24 Mar 2018 07:44:03 AEDT ]]> Cumulative effects of genetic markers and the detection of advanced colorectal neoplasias by population screening https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:26445 Sat 24 Mar 2018 07:27:17 AEDT ]]> cDNA analysis of the BRCA1 unclassified variant c.5194-12G > A (letter) https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:23714 Sat 24 Mar 2018 07:16:58 AEDT ]]> POU3F3-related disorder: Defining the phenotype and expanding the molecular spectrum https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:52838 Mon 30 Oct 2023 09:41:00 AEDT ]]>