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Terminal deletion of chromosome 10p13 as a cause of hypoparathyroidism in a neonate /unibl/sci/idNaucniRad:22945 https://dx.doi.org/10.5457/p2005-114.204 Academic Article text 2018 Н. Марић, G. Bukara-Radujković, Љ. Соломун, Д. Јојић, Terminal deletion of chromosome 10p13 as a cause of hypoparathyroidism in a neonate, Central European Journal of Paediatrics, Vol. 14, No. 1, pp. 88 - 91, 2018 https://cejpaediatrics.com/index.php/cejp/article/view/310/pdf 88 91 Central European Journal of Paediatrics 2490-3671 /unibl/author/Nina Marić https://www.unibl.org/sr-lat/fis/zaposlen/3384-gordana-bukara-radujkovic /unibl/author/Ljilja Solomun https://www.unibl.org/sr-lat/fis/zaposlen/3383-dragica-jojic https://med.unibl.org https://med.unibl.org Central European Journal of Paediatrics 2490-3671 91 88 /unibl/author/Nina Marić https://www.unibl.org/sr-lat/fis/zaposlen/3384-gordana-bukara-radujkovic /unibl/author/Ljilja Solomun https://www.unibl.org/sr-lat/fis/zaposlen/3383-dragica-jojic https://pub.unibl.org/s/cir/item/39665