Kaya, D. Et Al. 2024. A case report of a patient with neurodevelopmental disorder with impaired speech and hyperkinetic movements: A biallelic variant in the ZNF142 gene. American Journal of Medical Genetics, Part A , vol.194, no.9 .

Kaya, D., CEYLAN KÖSE, C., AKCAN, M. B., & SILAN, F., (2024). A case report of a patient with neurodevelopmental disorder with impaired speech and hyperkinetic movements: A biallelic variant in the ZNF142 gene. American Journal of Medical Genetics, Part A , vol.194, no.9.

Kaya, DERYA Et Al. "A case report of a patient with neurodevelopmental disorder with impaired speech and hyperkinetic movements: A biallelic variant in the ZNF142 gene," American Journal of Medical Genetics, Part A , vol.194, no.9, 2024

Kaya, DERYA Et Al. "A case report of a patient with neurodevelopmental disorder with impaired speech and hyperkinetic movements: A biallelic variant in the ZNF142 gene." American Journal of Medical Genetics, Part A , vol.194, no.9, 2024

Kaya, D. Et Al. (2024) . "A case report of a patient with neurodevelopmental disorder with impaired speech and hyperkinetic movements: A biallelic variant in the ZNF142 gene." American Journal of Medical Genetics, Part A , vol.194, no.9.

@article{article, author={DERYA KAYA Et Al. }, title={A case report of a patient with neurodevelopmental disorder with impaired speech and hyperkinetic movements: A biallelic variant in the ZNF142 gene}, journal={American Journal of Medical Genetics, Part A}, year=2024}