<Record><identifier xmlns="http://purl.org/dc/elements/1.1/">URN:NBN:SI:doc-YHUA485U</identifier><date>2012</date><creator>Erjavec Škerget, Alenka</creator><creator>Kokalj-Vokač, Nadja</creator><creator>Kunčnik, Vesna</creator><creator>Stangler Herodež, Špela</creator><creator>Zagradišnik, Boris</creator><relation>documents/doc/Y/URN_NBN_SI_doc-YHUA485U_001.pdf</relation><relation>documents/doc/Y/URN_NBN_SI_doc-YHUA485U_001.txt</relation><format format_type="issue">1</format><format format_type="volume">19</format><format format_type="type">article</format><format format_type="extent">str. 26-34</format><identifier identifier_type="ISSN">1318-4423</identifier><identifier identifier_type="COBISSID">4271423</identifier><identifier identifier_type="URN">URN:NBN:SI:doc-YHUA485U</identifier><language>slv</language><publisher publisher_location="Ljubljana">Združenje pediatrov Slovenije</publisher><publisher publisher_location="Ljubljana">Združenje specialistov šolske in visokošolske medicine Slovenije</publisher><source>Slovenska pediatrija</source><rights>BY-NC</rights><subject language_type_id="slv">Abnormalities</subject><subject language_type_id="slv">Diagnosis</subject><subject language_type_id="slv">Diagnostika</subject><subject language_type_id="slv">Duševna manjrazvitost</subject><subject language_type_id="slv">duševne motnje</subject><subject language_type_id="slv">Fragile X Syndrome</subject><subject language_type_id="slv">Fragilni X sindrom</subject><subject language_type_id="slv">Genetics</subject><subject language_type_id="slv">Genetika</subject><subject language_type_id="slv">Kromosom X</subject><subject language_type_id="slv">Mental Retardation</subject><subject language_type_id="slv">Nepravilnosti</subject><subject language_type_id="slv">Reverse Transcriptase Polymerase Chain Reaction</subject><subject language_type_id="slv">sindrom fragilnega kromosoma</subject><subject language_type_id="slv">Verižna reakcija s polimerazo</subject><subject language_type_id="slv">X Chromosome</subject><title>Odkrivanje sindroma fragilnega kromosoma X na osnovi tehnologije PCR pri moški populaciji iz severovzhodne Slovenije</title><title>Detection of fragile X syndrome based on PCR technology in the male population of north-eastern Slovenia</title></Record>