Yeter, B. Et Al. 2022. A novel mutation in the TRIP11 gene: Diagnostic approach from relatively common skeletal dysplasias to an extremely rare Odontochondrodysplasia.. Journal of clinical research in pediatric endocrinology , vol.14 , 475-480.

Yeter, B., Dilruba Aslanger, A., Yesil, G., & Elcioglu, N. H., (2022). A novel mutation in the TRIP11 gene: Diagnostic approach from relatively common skeletal dysplasias to an extremely rare Odontochondrodysplasia.. Journal of clinical research in pediatric endocrinology , vol.14, 475-480.

Yeter, Burcu Et Al. "A novel mutation in the TRIP11 gene: Diagnostic approach from relatively common skeletal dysplasias to an extremely rare Odontochondrodysplasia.," Journal of clinical research in pediatric endocrinology , vol.14, 475-480, 2022

Yeter, Burcu Et Al. "A novel mutation in the TRIP11 gene: Diagnostic approach from relatively common skeletal dysplasias to an extremely rare Odontochondrodysplasia.." Journal of clinical research in pediatric endocrinology , vol.14, pp.475-480, 2022

Yeter, B. Et Al. (2022) . "A novel mutation in the TRIP11 gene: Diagnostic approach from relatively common skeletal dysplasias to an extremely rare Odontochondrodysplasia.." Journal of clinical research in pediatric endocrinology , vol.14, pp.475-480.

@article{article, author={Burcu Yeter Et Al. }, title={A novel mutation in the TRIP11 gene: Diagnostic approach from relatively common skeletal dysplasias to an extremely rare Odontochondrodysplasia.}, journal={Journal of clinical research in pediatric endocrinology}, year=2022, pages={475-480} }