Yüce Kahraman, Ç. Et Al. 2019. A novel mutation of a rare genetic condition: Primary hypertrophic osteoarthropathy. 13.BALKAN GENETİK KONGRESİ , (Edirne, Turkey), 63.

Yüce Kahraman, Ç., Orbak, Z., Tatar, A., Yakar, Ö., Cinkara, N., & Ercoşkun, P., (2019). A novel mutation of a rare genetic condition: Primary hypertrophic osteoarthropathy . 13.BALKAN GENETİK KONGRESİ (pp.63). Edirne, Turkey

Yüce Kahraman, Çiğdem Et Al. "A novel mutation of a rare genetic condition: Primary hypertrophic osteoarthropathy," 13.BALKAN GENETİK KONGRESİ, Edirne, Turkey, 2019

Yüce Kahraman, Çiğdem Y. Et Al. "A novel mutation of a rare genetic condition: Primary hypertrophic osteoarthropathy." 13.BALKAN GENETİK KONGRESİ , Edirne, Turkey, pp.63, 2019

Yüce Kahraman, Ç. Et Al. (2019) . "A novel mutation of a rare genetic condition: Primary hypertrophic osteoarthropathy." 13.BALKAN GENETİK KONGRESİ , Edirne, Turkey, p.63.

@conferencepaper{conferencepaper, author={Çiğdem YÜCE KAHRAMAN Et Al. }, title={A novel mutation of a rare genetic condition: Primary hypertrophic osteoarthropathy}, congress name={13.BALKAN GENETİK KONGRESİ}, city={Edirne}, country={Turkey}, year={2019}, pages={63} }