Kaya, M. Et Al. 2022. Kenny-Caffey Syndrome Type 2: Clinical And Molecular Features In Four Unrelated Patients And Report Of A Novel Fam111A Variant. 15. Ulusal Tıbbi Genetik Kongresi , (Muğla, Turkey), 272.

Kaya, M., Eviz, E., Koçak Eker, H., Tekmenüray Ünal, A., Türkyılmaz, A., Çepni, E., ... Çayır, A.(2022). Kenny-Caffey Syndrome Type 2: Clinical And Molecular Features In Four Unrelated Patients And Report Of A Novel Fam111A Variant . 15. Ulusal Tıbbi Genetik Kongresi (pp.272). Muğla, Turkey

Kaya, Mert Et Al. "Kenny-Caffey Syndrome Type 2: Clinical And Molecular Features In Four Unrelated Patients And Report Of A Novel Fam111A Variant," 15. Ulusal Tıbbi Genetik Kongresi, Muğla, Turkey, 2022

Kaya, Mert Et Al. "Kenny-Caffey Syndrome Type 2: Clinical And Molecular Features In Four Unrelated Patients And Report Of A Novel Fam111A Variant." 15. Ulusal Tıbbi Genetik Kongresi , Muğla, Turkey, pp.272, 2022

Kaya, M. Et Al. (2022) . "Kenny-Caffey Syndrome Type 2: Clinical And Molecular Features In Four Unrelated Patients And Report Of A Novel Fam111A Variant." 15. Ulusal Tıbbi Genetik Kongresi , Muğla, Turkey, p.272.

@conferencepaper{conferencepaper, author={Mert Kaya Et Al. }, title={Kenny-Caffey Syndrome Type 2: Clinical And Molecular Features In Four Unrelated Patients And Report Of A Novel Fam111A Variant}, congress name={15. Ulusal Tıbbi Genetik Kongresi}, city={Muğla}, country={Turkey}, year={2022}, pages={272} }