<Record><identifier xmlns="http://purl.org/dc/elements/1.1/">URN:NBN:SI:DOC-29DLBGMZ</identifier><date>2012</date><creator>Milatovič, Maša</creator><creator>Novaković, Srdjan</creator><creator>Prosenc, Uršula</creator><relation>documents/doc/2/URN_NBN_SI_doc-29DLBGMZ_001.pdf</relation><relation>documents/doc/2/URN_NBN_SI_doc-29DLBGMZ_001.txt</relation><format format_type="volume">16</format><format format_type="issue">2</format><format format_type="type">article</format><format format_type="extent">str. 87-89, 113</format><identifier identifier_type="ISSN">1408-1741</identifier><identifier identifier_type="COBISSID">1423995</identifier><identifier identifier_type="URN">URN:NBN:SI:doc-29DLBGMZ</identifier><language>slv</language><publisher>Onkološki inštitut Ljubljana</publisher><source>Onkologija (Ljubljana)</source><rights>BY</rights><subject language_type_id="eng">Genetics</subject><subject language_type_id="slv">genetika</subject><subject language_type_id="slv">genetski testi</subject><subject language_type_id="eng">Hipper-Lindau disease</subject><subject language_type_id="slv">mutacije</subject><subject language_type_id="eng">Mutation</subject><title>določanje mutacij v genu VHL</title><title>Odkrivanje dednega sindroma von Hippel-Lindau</title></Record>