Ergoren, M. C. Et Al. 2022. Characterization of a Novel Frameshift Mutation Within the TRPS1 Gene Causing Trichorhinophalangeal Syndrome Type 1 in a Kindred Cypriot Family.. Applied immunohistochemistry & molecular morphology : AIMM , vol.30, no.9 , 635-639.

Ergoren, M. C., Akcan, N., Manara, E., Paolacci, S., Fahrioğlu, U., Betmezoglu, M., ... Bundak, R.(2022). Characterization of a Novel Frameshift Mutation Within the TRPS1 Gene Causing Trichorhinophalangeal Syndrome Type 1 in a Kindred Cypriot Family.. Applied immunohistochemistry & molecular morphology : AIMM , vol.30, no.9, 635-639.

Ergoren, Mahmut Et Al. "Characterization of a Novel Frameshift Mutation Within the TRPS1 Gene Causing Trichorhinophalangeal Syndrome Type 1 in a Kindred Cypriot Family.," Applied immunohistochemistry & molecular morphology : AIMM , vol.30, no.9, 635-639, 2022

Ergoren, Mahmut C. Et Al. "Characterization of a Novel Frameshift Mutation Within the TRPS1 Gene Causing Trichorhinophalangeal Syndrome Type 1 in a Kindred Cypriot Family.." Applied immunohistochemistry & molecular morphology : AIMM , vol.30, no.9, pp.635-639, 2022

Ergoren, M. C. Et Al. (2022) . "Characterization of a Novel Frameshift Mutation Within the TRPS1 Gene Causing Trichorhinophalangeal Syndrome Type 1 in a Kindred Cypriot Family.." Applied immunohistochemistry & molecular morphology : AIMM , vol.30, no.9, pp.635-639.

@article{article, author={Mahmut Cerkez Ergoren Et Al. }, title={Characterization of a Novel Frameshift Mutation Within the TRPS1 Gene Causing Trichorhinophalangeal Syndrome Type 1 in a Kindred Cypriot Family.}, journal={Applied immunohistochemistry & molecular morphology : AIMM}, year=2022, pages={635-639} }