A Novel Mutation in the TRIP11 Gene: Diagnostic Approach from Relatively Common Skeletal Dysplasias to an Extremely Rare Odontochondrodysplasia.


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Yeter B., Dilruba Aslanger A. D., Yesil G., Elcioglu N. H.

Journal of clinical research in pediatric endocrinology, vol.14, no.4, pp.475-480, 2022 (SCI-Expanded) identifier identifier