SARIKAYA, E. Et Al. 2022. A very rare cause of arthrogryposis multiplex congenita: a novel mutation in TOR1A. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.35, no.6 , 845-850.

SARIKAYA, E., ÖZÇELİK, 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 & METABOLISM , vol.35, no.6, 845-850.

SARIKAYA, EMRE Et Al. "A very rare cause of arthrogryposis multiplex congenita: a novel mutation in TOR1A," JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.35, no.6, 845-850, 2022

SARIKAYA, EMRE Et Al. "A very rare cause of arthrogryposis multiplex congenita: a novel mutation in TOR1A." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.35, no.6, pp.845-850, 2022

SARIKAYA, E. Et Al. (2022) . "A very rare cause of arthrogryposis multiplex congenita: a novel mutation in TOR1A." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.35, no.6, pp.845-850.

@article{article, author={EMRE SARIKAYA Et Al. }, title={A very rare cause of arthrogryposis multiplex congenita: a novel mutation in TOR1A}, journal={JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM}, year=2022, pages={845-850} }