pid,type,title,authors,mentors,source_title,published_date,url,doi,isbn,issn,eissn
zvu:8016,thesis,Fenilketonurija,"Ponjan, Andrea",,,,,,,,
zvu:7954,thesis,"Fragilni X sindrom","Posedi, Melani",,,,,,,,
zvu:6885,thesis,"Bolesti sa X - vezanim nasljeđivanjem","Kovak, Laura",,,,,,,,
zvu:6888,thesis,"Prenatalna genetska dijagnostika","Mihalinec, Dorotea",,,,,,,,
mef:4792,"journal article","The landscape of Mucopolysaccharidosis in Southern and Eastern European countries: a survey from 19 specialistic centers","Tylki-Szymańska, Anna; Almássy, Zsuzsanna; Christophidou-Anastasiadou, Violetta; Avdjieva-Tzavella, Daniela; Barišić, Ingeborg; Cerkauskiene, Rimante; Cuturilo, Goran; Djiordjevic, Maja; Gucev, Zoran; Hlavata, Anna; Kieć-Wilk, Beata; Magner, Martin; Pećin, Ivan; Plaiasu, Vasilica; Samardzic, Mira; Zafeiriou, Dimitrios; Zaganas, Ioannis; Lampe, Christina",,,,,,,,
zvu:3592,thesis,"Genotipsko fenotipska korelacija u hrvatskih bolesnika oboljelih od cistične fibroze","Vlašić, Marcela",,,,,,,,
zvu:3593,thesis,"Sindrom delecije 22q11.2 u skupini hrvatskih bolesnika","Matjačić, Ivana",,,,,,,,
pharma:532,thesis,"Validacija metode za probir dinamičkih mutacija u genu FMR1","Škrlec, Ivana",,,,,,,,
pharma:379,dissertation,"Influence of genetic and environmental factors on N-glycosylation of immunoglobulin G and total plasma proteins determined by twin study","Keser, Toma",,,,,,,,
mef:8040,"journal article","Osteogenesis imperfecta - multi-systemic and life-long disease that affects whole family ","Primorac, Dragan; Antičević, Darko; Barišić, Ingeborg; Hudetz, Damir; Ivković, Alan",,,,,,,,
pharma:329,dissertation,"Asimetrični dimetilarginin u bubrežnoj varijanti Fabryjeve bolesti","Škrbec, Alen",,,,,,,,