Demirel, G. Et Al. 2012. A CASE OF KEUTEL SYNDROME DIAGNOSED IN THE NEONATAL PERIOD: ASSOCIATED WITH BINDER PHENOTYPE. GENETIC COUNSELING , vol.23, no.1 , 25-30.

Demirel, G., Oguz, S. S., Celik, I. H., Erdeve, Ö., Uras, N., & Dilmen, U., (2012). A CASE OF KEUTEL SYNDROME DIAGNOSED IN THE NEONATAL PERIOD: ASSOCIATED WITH BINDER PHENOTYPE. GENETIC COUNSELING , vol.23, no.1, 25-30.

Demirel, G. Et Al. "A CASE OF KEUTEL SYNDROME DIAGNOSED IN THE NEONATAL PERIOD: ASSOCIATED WITH BINDER PHENOTYPE," GENETIC COUNSELING , vol.23, no.1, 25-30, 2012

Demirel, G. Et Al. "A CASE OF KEUTEL SYNDROME DIAGNOSED IN THE NEONATAL PERIOD: ASSOCIATED WITH BINDER PHENOTYPE." GENETIC COUNSELING , vol.23, no.1, pp.25-30, 2012

Demirel, G. Et Al. (2012) . "A CASE OF KEUTEL SYNDROME DIAGNOSED IN THE NEONATAL PERIOD: ASSOCIATED WITH BINDER PHENOTYPE." GENETIC COUNSELING , vol.23, no.1, pp.25-30.

@article{article, author={G. Demirel Et Al. }, title={A CASE OF KEUTEL SYNDROME DIAGNOSED IN THE NEONATAL PERIOD: ASSOCIATED WITH BINDER PHENOTYPE}, journal={GENETIC COUNSELING}, year=2012, pages={25-30} }