A. O. ÇAĞLAYAN Et Al. , "A PROVISIONALLY UNIQUE SYNDROME WITH FEATURES INCLUDING "MOLAR TOOTH" SIGN AND "FEMORAL HYPOPLASIA"," GENETIC COUNSELING , vol.20, no.4, pp.359-365, 2009
ÇAĞLAYAN, A. O. Et Al. 2009. A PROVISIONALLY UNIQUE SYNDROME WITH FEATURES INCLUDING "MOLAR TOOTH" SIGN AND "FEMORAL HYPOPLASIA". GENETIC COUNSELING , vol.20, no.4 , 359-365.
ÇAĞLAYAN, A. O., Gumus, H., Yikilmaz, A., Gumus, G. O., & Per, H., (2009). A PROVISIONALLY UNIQUE SYNDROME WITH FEATURES INCLUDING "MOLAR TOOTH" SIGN AND "FEMORAL HYPOPLASIA". GENETIC COUNSELING , vol.20, no.4, 359-365.
ÇAĞLAYAN, AHMET Et Al. "A PROVISIONALLY UNIQUE SYNDROME WITH FEATURES INCLUDING "MOLAR TOOTH" SIGN AND "FEMORAL HYPOPLASIA"," GENETIC COUNSELING , vol.20, no.4, 359-365, 2009
ÇAĞLAYAN, AHMET O. Et Al. "A PROVISIONALLY UNIQUE SYNDROME WITH FEATURES INCLUDING "MOLAR TOOTH" SIGN AND "FEMORAL HYPOPLASIA"." GENETIC COUNSELING , vol.20, no.4, pp.359-365, 2009
ÇAĞLAYAN, A. O. Et Al. (2009) . "A PROVISIONALLY UNIQUE SYNDROME WITH FEATURES INCLUDING "MOLAR TOOTH" SIGN AND "FEMORAL HYPOPLASIA"." GENETIC COUNSELING , vol.20, no.4, pp.359-365.
@article{article, author={AHMET OKAY ÇAĞLAYAN Et Al. }, title={A PROVISIONALLY UNIQUE SYNDROME WITH FEATURES INCLUDING "MOLAR TOOTH" SIGN AND "FEMORAL HYPOPLASIA"}, journal={GENETIC COUNSELING}, year=2009, pages={359-365} }