B. Yeter 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, no.4, 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, no.4 , 475-480.
Yeter, B., Dilruba Aslanger, A. D., 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, no.4, 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, no.4, 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, no.4, 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, no.4, 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} }