TÜRKYILMAZ, A. Et Al. 2016. A case of Weaver Syndrome caused by a novel frameshift EZH2 mutation. European Society of Human Genetics .

TÜRKYILMAZ, A., KARAKAYA, T., ŞİMŞEK, H., SÖYLEMEZ, M. A., GEÇKİNLİ, B. B., ARMAN, A., ... DELİL, K.(2016). A case of Weaver Syndrome caused by a novel frameshift EZH2 mutation . European Society of Human Genetics

TÜRKYILMAZ, AYBERK Et Al. "A case of Weaver Syndrome caused by a novel frameshift EZH2 mutation," European Society of Human Genetics, 2016

TÜRKYILMAZ, AYBERK Et Al. "A case of Weaver Syndrome caused by a novel frameshift EZH2 mutation." European Society of Human Genetics , 2016

TÜRKYILMAZ, A. Et Al. (2016) . "A case of Weaver Syndrome caused by a novel frameshift EZH2 mutation." European Society of Human Genetics .

@conferencepaper{conferencepaper, author={AYBERK TÜRKYILMAZ Et Al. }, title={A case of Weaver Syndrome caused by a novel frameshift EZH2 mutation}, congress name={European Society of Human Genetics}, city={}, country={}, year={2016}}