Turkyilmaz, A. Et Al. 2020. FGF3-Related Phenotypes: A Study of LAMM Syndrome and Otodental Dysplasia Patients with Two Novel Mutations in FGF3 Gene. INTERNATIONAL JOURNAL OF HUMAN GENETICS , vol.20, no.4 , 179-190.

Turkyilmaz, A., GEÇKİNLİ, B. B., ALAVANDA, C., Zengin, G., Ates, E. A., & ARMAN, A., (2020). FGF3-Related Phenotypes: A Study of LAMM Syndrome and Otodental Dysplasia Patients with Two Novel Mutations in FGF3 Gene. INTERNATIONAL JOURNAL OF HUMAN GENETICS , vol.20, no.4, 179-190.

Turkyilmaz, AYBERK Et Al. "FGF3-Related Phenotypes: A Study of LAMM Syndrome and Otodental Dysplasia Patients with Two Novel Mutations in FGF3 Gene," INTERNATIONAL JOURNAL OF HUMAN GENETICS , vol.20, no.4, 179-190, 2020

Turkyilmaz, AYBERK Et Al. "FGF3-Related Phenotypes: A Study of LAMM Syndrome and Otodental Dysplasia Patients with Two Novel Mutations in FGF3 Gene." INTERNATIONAL JOURNAL OF HUMAN GENETICS , vol.20, no.4, pp.179-190, 2020

Turkyilmaz, A. Et Al. (2020) . "FGF3-Related Phenotypes: A Study of LAMM Syndrome and Otodental Dysplasia Patients with Two Novel Mutations in FGF3 Gene." INTERNATIONAL JOURNAL OF HUMAN GENETICS , vol.20, no.4, pp.179-190.

@article{article, author={AYBERK TÜRKYILMAZ Et Al. }, title={FGF3-Related Phenotypes: A Study of LAMM Syndrome and Otodental Dysplasia Patients with Two Novel Mutations in FGF3 Gene}, journal={INTERNATIONAL JOURNAL OF HUMAN GENETICS}, year=2020, pages={179-190} }