Bayram, A. K. Et Al. 2015. A rare case of congenital fibrosis of extraocular muscle type IA due to KIF2IA mutation with Marcus Gunn jaw-winking phenomenon. EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.19, no.6 , 743-746.

Bayram, A. K., PER, H., Quon, J., CANPOLAT, M., Uelgen, E., Dogan, H., ... GÜMÜŞ, H.(2015). A rare case of congenital fibrosis of extraocular muscle type IA due to KIF2IA mutation with Marcus Gunn jaw-winking phenomenon. EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.19, no.6, 743-746.

Bayram, Ayse Et Al. "A rare case of congenital fibrosis of extraocular muscle type IA due to KIF2IA mutation with Marcus Gunn jaw-winking phenomenon," EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.19, no.6, 743-746, 2015

Bayram, Ayse K. Et Al. "A rare case of congenital fibrosis of extraocular muscle type IA due to KIF2IA mutation with Marcus Gunn jaw-winking phenomenon." EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.19, no.6, pp.743-746, 2015

Bayram, A. K. Et Al. (2015) . "A rare case of congenital fibrosis of extraocular muscle type IA due to KIF2IA mutation with Marcus Gunn jaw-winking phenomenon." EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.19, no.6, pp.743-746.

@article{article, author={Ayse Kacar Bayram Et Al. }, title={A rare case of congenital fibrosis of extraocular muscle type IA due to KIF2IA mutation with Marcus Gunn jaw-winking phenomenon}, journal={EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY}, year=2015, pages={743-746} }