KÖR, D. Et Al. 2016. Two siblings with neonatal onset Dubin Johnson syndrome and hypothyroidism harboring a novel mutation in the ABCC2 gene. SSIEM 2016 ROME .

KÖR, D., ŞEKER YILMAZ, B., BULUT, F. D., CEYLANER, S., TOPALOĞLU, A. K., & ÖNENLİ MUNGAN, H. N., (2016). Two siblings with neonatal onset Dubin Johnson syndrome and hypothyroidism harboring a novel mutation in the ABCC2 gene . SSIEM 2016 ROME

KÖR, DENİZ Et Al. "Two siblings with neonatal onset Dubin Johnson syndrome and hypothyroidism harboring a novel mutation in the ABCC2 gene," SSIEM 2016 ROME, 2016

KÖR, DENİZ Et Al. "Two siblings with neonatal onset Dubin Johnson syndrome and hypothyroidism harboring a novel mutation in the ABCC2 gene." SSIEM 2016 ROME , 2016

KÖR, D. Et Al. (2016) . "Two siblings with neonatal onset Dubin Johnson syndrome and hypothyroidism harboring a novel mutation in the ABCC2 gene." SSIEM 2016 ROME .

@conferencepaper{conferencepaper, author={DENİZ KOR Et Al. }, title={Two siblings with neonatal onset Dubin Johnson syndrome and hypothyroidism harboring a novel mutation in the ABCC2 gene}, congress name={SSIEM 2016 ROME}, city={}, country={}, year={2016}}