M. C. Ergoren 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 , 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 , vol.30, no.9 , 635-639.
Ergoren, M. C., Akcan, N., Manara, E., Paolacci, S., Fahrioglu, 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 , 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 , 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 , 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 , 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}, year=2022, pages={635-639} }