GÜRSOY, S. Et Al. 2019. The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome. Turkish Journal of Pediatrics , vol.61, no.4 , 589-593.

GÜRSOY, S., Kutbay, Y. B., Özdemir, T. R., & Hazan, F., (2019). The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome. Turkish Journal of Pediatrics , vol.61, no.4, 589-593.

GÜRSOY, SEMRA Et Al. "The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome," Turkish Journal of Pediatrics , vol.61, no.4, 589-593, 2019

GÜRSOY, SEMRA Et Al. "The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome." Turkish Journal of Pediatrics , vol.61, no.4, pp.589-593, 2019

GÜRSOY, S. Et Al. (2019) . "The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome." Turkish Journal of Pediatrics , vol.61, no.4, pp.589-593.

@article{article, author={SEMRA GÜRSOY Et Al. }, title={The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome}, journal={Turkish Journal of Pediatrics}, year=2019, pages={589-593} }