Cammarata-Scalisi, F. Et Al. 2019. Clinical and genetic findings of two cases with Apert syndrome.. Boletin medico del Hospital Infantil de Mexico , vol.76 , 44-48.

Cammarata-Scalisi, F., Yilmaz, E., Callea, M., Avendaño, A., Mıhçı, E., & Alper, O. M., (2019). Clinical and genetic findings of two cases with Apert syndrome.. Boletin medico del Hospital Infantil de Mexico , vol.76, 44-48.

Cammarata-Scalisi, Francisco Et Al. "Clinical and genetic findings of two cases with Apert syndrome.," Boletin medico del Hospital Infantil de Mexico , vol.76, 44-48, 2019

Cammarata-Scalisi, Francisco Et Al. "Clinical and genetic findings of two cases with Apert syndrome.." Boletin medico del Hospital Infantil de Mexico , vol.76, pp.44-48, 2019

Cammarata-Scalisi, F. Et Al. (2019) . "Clinical and genetic findings of two cases with Apert syndrome.." Boletin medico del Hospital Infantil de Mexico , vol.76, pp.44-48.

@article{article, author={Francisco Cammarata-Scalisi Et Al. }, title={Clinical and genetic findings of two cases with Apert syndrome.}, journal={Boletin medico del Hospital Infantil de Mexico}, year=2019, pages={44-48} }