<Record><identifier xmlns="http://purl.org/dc/elements/1.1/">URN:NBN:SI:doc-PR88FX5R</identifier><date>2003</date><creator>Centurión, Santiago A.</creator><creator>Schwartz, Robert A.</creator><relation>documents/doc/P/URN_NBN_SI_doc-PR88FX5R_001.pdf</relation><relation>documents/doc/P/URN_NBN_SI_doc-PR88FX5R_001.txt</relation><format format_type="issue">1</format><format format_type="volume">12</format><format format_type="type">article</format><format format_type="extent">str. 32-36</format><identifier identifier_type="ISSN">1318-4458</identifier><identifier identifier_type="COBISSID">16238553</identifier><identifier identifier_type="URN">URN:NBN:SI:doc-PR88FX5R</identifier><language>eng</language><publisher>Slovene Welding Society</publisher><source>Acta dermatovenerologica Alpina, Pannonica et Adriatica</source><rights>InC</rights><subject language_type_id="eng">Albinism, Oculocutaneous</subject><subject language_type_id="slv">Albinizem okulokutani</subject><subject language_type_id="eng">Angelman Syndrome</subject><subject language_type_id="slv">Angelmanov sindrom</subject><subject language_type_id="slv">Chediak-Hagashijev sindrom</subject><subject language_type_id="eng">Chediak-Higashi Syndrome</subject><subject language_type_id="slv">dermatologija</subject><subject language_type_id="eng">Diagnosis</subject><subject language_type_id="eng">diagnostika</subject><subject language_type_id="slv">etiologija</subject><subject language_type_id="slv">kožne bolezni</subject><subject language_type_id="eng">Pathology</subject><subject language_type_id="eng">Prader-Willi Syndrome</subject><subject language_type_id="slv">Prader-Willijev sindrom</subject><subject language_type_id="eng">Therapy</subject><title>Oculocutaneous albinism type 2</title></Record>