Kayhan, G. Et Al. 2022. A Novel Homozygous Frameshift Mutation in the PLCB4 Gene Associated with Auriculocondylar Syndrome 2 and Accompanied by Mild Intellectual Disability. Türkiye Klinikleri Journal of Case Reports , vol.30, no.4 , 258-262.

Kayhan, G., Kazan, H. H., Öztürk, K., Sezer, A., & Perçin, F. E., (2022). A Novel Homozygous Frameshift Mutation in the PLCB4 Gene Associated with Auriculocondylar Syndrome 2 and Accompanied by Mild Intellectual Disability. Türkiye Klinikleri Journal of Case Reports , vol.30, no.4, 258-262.

Kayhan, GÜLSÜM Et Al. "A Novel Homozygous Frameshift Mutation in the PLCB4 Gene Associated with Auriculocondylar Syndrome 2 and Accompanied by Mild Intellectual Disability," Türkiye Klinikleri Journal of Case Reports , vol.30, no.4, 258-262, 2022

Kayhan, GÜLSÜM Et Al. "A Novel Homozygous Frameshift Mutation in the PLCB4 Gene Associated with Auriculocondylar Syndrome 2 and Accompanied by Mild Intellectual Disability." Türkiye Klinikleri Journal of Case Reports , vol.30, no.4, pp.258-262, 2022

Kayhan, G. Et Al. (2022) . "A Novel Homozygous Frameshift Mutation in the PLCB4 Gene Associated with Auriculocondylar Syndrome 2 and Accompanied by Mild Intellectual Disability." Türkiye Klinikleri Journal of Case Reports , vol.30, no.4, pp.258-262.

@article{article, author={GÜLSÜM KAYHAN Et Al. }, title={A Novel Homozygous Frameshift Mutation in the PLCB4 Gene Associated with Auriculocondylar Syndrome 2 and Accompanied by Mild Intellectual Disability}, journal={Türkiye Klinikleri Journal of Case Reports}, year=2022, pages={258-262} }