ŞİMŞEK KİPER, P. Ö. Et Al. 2017. A novel homozygous ROGD1 mutation in two siblings with Kohlschutter-Tönz syndrome: A rare entity. European Society of Human Genetics Conference 2017 , (Kopenhag) .

ŞİMŞEK KİPER, P. Ö., ÜTİNE, G. E., Zschocke, J., & BODUROĞLU, O. K., (2017). A novel homozygous ROGD1 mutation in two siblings with Kohlschutter-Tönz syndrome: A rare entity . European Society of Human Genetics Conference 2017, Kopenhag

ŞİMŞEK KİPER, PELİN Et Al. "A novel homozygous ROGD1 mutation in two siblings with Kohlschutter-Tönz syndrome: A rare entity," European Society of Human Genetics Conference 2017, Kopenhag, 2017

ŞİMŞEK KİPER, PELİN Ö. Et Al. "A novel homozygous ROGD1 mutation in two siblings with Kohlschutter-Tönz syndrome: A rare entity." European Society of Human Genetics Conference 2017 , Kopenhag, 2017

ŞİMŞEK KİPER, P. Ö. Et Al. (2017) . "A novel homozygous ROGD1 mutation in two siblings with Kohlschutter-Tönz syndrome: A rare entity." European Society of Human Genetics Conference 2017 , Kopenhag.

@conferencepaper{conferencepaper, author={PELİN ÖZLEM ŞİMŞEK KİPER Et Al. }, title={A novel homozygous ROGD1 mutation in two siblings with Kohlschutter-Tönz syndrome: A rare entity}, congress name={European Society of Human Genetics Conference 2017}, city={Kopenhag}, country={}, year={2017}}