E. Sarlkaya Et Al. , "A very rare cause of arthrogryposis multiplex congenita: a novel mutation in TOR1A," Journal of Pediatric Endocrinology and Metabolism , vol.35, no.6, pp.845-850, 2022
Sarlkaya, E. Et Al. 2022. A very rare cause of arthrogryposis multiplex congenita: a novel mutation in TOR1A. Journal of Pediatric Endocrinology and Metabolism , vol.35, no.6 , 845-850.
Sarlkaya, E., Özçelik, F., GÜL ŞİRAZ, Ü., HATİPOĞLU, N., GÜNEŞ, T., & DÜNDAR, M., (2022). A very rare cause of arthrogryposis multiplex congenita: a novel mutation in TOR1A. Journal of Pediatric Endocrinology and Metabolism , vol.35, no.6, 845-850.
Sarlkaya, Emre Et Al. "A very rare cause of arthrogryposis multiplex congenita: a novel mutation in TOR1A," Journal of Pediatric Endocrinology and Metabolism , vol.35, no.6, 845-850, 2022
Sarlkaya, Emre Et Al. "A very rare cause of arthrogryposis multiplex congenita: a novel mutation in TOR1A." Journal of Pediatric Endocrinology and Metabolism , vol.35, no.6, pp.845-850, 2022
Sarlkaya, E. Et Al. (2022) . "A very rare cause of arthrogryposis multiplex congenita: a novel mutation in TOR1A." Journal of Pediatric Endocrinology and Metabolism , vol.35, no.6, pp.845-850.
@article{article, author={Emre Sarlkaya Et Al. }, title={A very rare cause of arthrogryposis multiplex congenita: a novel mutation in TOR1A}, journal={Journal of Pediatric Endocrinology and Metabolism}, year=2022, pages={845-850} }