Kiper, P. O. S. Et Al. 2017. A novel homozygous ROGD1 mutation in two siblings with kohlschutter-tonz syndrome: a rare entity. 50th European-Society-of-Human-Genetics (ESHG) Conference , (Copenhagen, Denmark), 346.

Kiper, P. O. S., Utine, G. E., Zschocke, J., & BODUROĞLU, O. K., (2017). A novel homozygous ROGD1 mutation in two siblings with kohlschutter-tonz syndrome: a rare entity . 50th European-Society-of-Human-Genetics (ESHG) Conference (pp.346). Copenhagen, Denmark

Kiper, P. Et Al. "A novel homozygous ROGD1 mutation in two siblings with kohlschutter-tonz syndrome: a rare entity," 50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 2017

Kiper, P. O. Et Al. "A novel homozygous ROGD1 mutation in two siblings with kohlschutter-tonz syndrome: a rare entity." 50th European-Society-of-Human-Genetics (ESHG) Conference , Copenhagen, Denmark, pp.346, 2017

Kiper, P. O. S. Et Al. (2017) . "A novel homozygous ROGD1 mutation in two siblings with kohlschutter-tonz syndrome: a rare entity." 50th European-Society-of-Human-Genetics (ESHG) Conference , Copenhagen, Denmark, p.346.

@conferencepaper{conferencepaper, author={P. O. Simsek Kiper Et Al. }, title={A novel homozygous ROGD1 mutation in two siblings with kohlschutter-tonz syndrome: a rare entity}, congress name={50th European-Society-of-Human-Genetics (ESHG) Conference}, city={Copenhagen}, country={Denmark}, year={2017}, pages={346} }