GÜNDÜZ, O. R. Et Al. 2022. A rare syndrome from Canakkale; Kindler Syndrome with loss of heterozygosity of FERMT1 gene region . 7. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi , (Kayseri, Turkey).

GÜNDÜZ, O. R., IŞIK MERMUTLU, S., CEYLAN KÖSE, C., & SILAN, F., (2022). A rare syndrome from Canakkale; Kindler Syndrome with loss of heterozygosity of FERMT1 gene region . 7. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Turkey

GÜNDÜZ, ONUR Et Al. "A rare syndrome from Canakkale; Kindler Syndrome with loss of heterozygosity of FERMT1 gene region ," 7. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Turkey, 2022

GÜNDÜZ, ONUR R. Et Al. "A rare syndrome from Canakkale; Kindler Syndrome with loss of heterozygosity of FERMT1 gene region ." 7. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi , Kayseri, Turkey, 2022

GÜNDÜZ, O. R. Et Al. (2022) . "A rare syndrome from Canakkale; Kindler Syndrome with loss of heterozygosity of FERMT1 gene region ." 7. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi , Kayseri, Turkey.

@conferencepaper{conferencepaper, author={ONUR RECEP GÜNDÜZ Et Al. }, title={A rare syndrome from Canakkale; Kindler Syndrome with loss of heterozygosity of FERMT1 gene region }, congress name={7. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi}, city={Kayseri}, country={Turkey}, year={2022}}