Taylan, F. Et Al. 2017. Two novel mutations in XYLT2 cause spondyloocular syndrome.. American journal of medical genetics. Part A , vol.173, no.12 , 3195-3200.

Taylan, F., Abali, Z. Y., Jaentti, N., Gunes, N., Darendeliler, F. F., Bas, F., ... Poyrazoglu, Ş.(2017). Two novel mutations in XYLT2 cause spondyloocular syndrome.. American journal of medical genetics. Part A , vol.173, no.12, 3195-3200.

Taylan, Fulya Et Al. "Two novel mutations in XYLT2 cause spondyloocular syndrome.," American journal of medical genetics. Part A , vol.173, no.12, 3195-3200, 2017

Taylan, Fulya Et Al. "Two novel mutations in XYLT2 cause spondyloocular syndrome.." American journal of medical genetics. Part A , vol.173, no.12, pp.3195-3200, 2017

Taylan, F. Et Al. (2017) . "Two novel mutations in XYLT2 cause spondyloocular syndrome.." American journal of medical genetics. Part A , vol.173, no.12, pp.3195-3200.

@article{article, author={Fulya Taylan Et Al. }, title={Two novel mutations in XYLT2 cause spondyloocular syndrome.}, journal={American journal of medical genetics. Part A}, year=2017, pages={3195-3200} }