Cetin, Z. Et Al. 2016. A MOLECULARLY CHARACTERIZED INTERSTITIAL DELETION ENCOPASSING THE 11q14.1-q23.3 REGION IN A CASE WITH MULTIPLE CONGENITAL ABNORMALITIES. GENETIC COUNSELING , vol.27, no.1 , 51-66.

Cetin, Z., ALTIOK-CLARK, O., Yakut, S., GUZEL-NUR, B., MIHÇI, E., & Berker-Karauzum, S., (2016). A MOLECULARLY CHARACTERIZED INTERSTITIAL DELETION ENCOPASSING THE 11q14.1-q23.3 REGION IN A CASE WITH MULTIPLE CONGENITAL ABNORMALITIES. GENETIC COUNSELING , vol.27, no.1, 51-66.

Cetin, Z. Et Al. "A MOLECULARLY CHARACTERIZED INTERSTITIAL DELETION ENCOPASSING THE 11q14.1-q23.3 REGION IN A CASE WITH MULTIPLE CONGENITAL ABNORMALITIES," GENETIC COUNSELING , vol.27, no.1, 51-66, 2016

Cetin, Z. Et Al. "A MOLECULARLY CHARACTERIZED INTERSTITIAL DELETION ENCOPASSING THE 11q14.1-q23.3 REGION IN A CASE WITH MULTIPLE CONGENITAL ABNORMALITIES." GENETIC COUNSELING , vol.27, no.1, pp.51-66, 2016

Cetin, Z. Et Al. (2016) . "A MOLECULARLY CHARACTERIZED INTERSTITIAL DELETION ENCOPASSING THE 11q14.1-q23.3 REGION IN A CASE WITH MULTIPLE CONGENITAL ABNORMALITIES." GENETIC COUNSELING , vol.27, no.1, pp.51-66.

@article{article, author={Z. Cetin Et Al. }, title={A MOLECULARLY CHARACTERIZED INTERSTITIAL DELETION ENCOPASSING THE 11q14.1-q23.3 REGION IN A CASE WITH MULTIPLE CONGENITAL ABNORMALITIES}, journal={GENETIC COUNSELING}, year=2016, pages={51-66} }