Ergin, R. N. Et Al. 2015. A VARIANT CASE OF 6p24 DELETION SYNDROME (OMIM #612582). GENETIC COUNSELING , vol.26, no.2 , 237-241.

Ergin, R. N., Cigerciogullari, E., Alanay, Y., & Yayla, M., (2015). A VARIANT CASE OF 6p24 DELETION SYNDROME (OMIM #612582). GENETIC COUNSELING , vol.26, no.2, 237-241.

Ergin, R. Et Al. "A VARIANT CASE OF 6p24 DELETION SYNDROME (OMIM #612582)," GENETIC COUNSELING , vol.26, no.2, 237-241, 2015

Ergin, R. N. Et Al. "A VARIANT CASE OF 6p24 DELETION SYNDROME (OMIM #612582)." GENETIC COUNSELING , vol.26, no.2, pp.237-241, 2015

Ergin, R. N. Et Al. (2015) . "A VARIANT CASE OF 6p24 DELETION SYNDROME (OMIM #612582)." GENETIC COUNSELING , vol.26, no.2, pp.237-241.

@article{article, author={R. N. Ergin Et Al. }, title={A VARIANT CASE OF 6p24 DELETION SYNDROME (OMIM #612582)}, journal={GENETIC COUNSELING}, year=2015, pages={237-241} }