Cebi, A. H. Et Al. 2018. Whole exome sequencing helps the diagnosis of two siblings with SLC19A3 mutation. 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) , (Milan, Italy), 972-973.

Cebi, A. H., Kamasak, T., Seyhan, S., Yilmaz, H. O., & Cansu, A., (2018). Whole exome sequencing helps the diagnosis of two siblings with SLC19A3 mutation . 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) (pp.972-973). Milan, Italy

Cebi, ALPER Et Al. "Whole exome sequencing helps the diagnosis of two siblings with SLC19A3 mutation," 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 2018

Cebi, ALPER H. Et Al. "Whole exome sequencing helps the diagnosis of two siblings with SLC19A3 mutation." 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) , Milan, Italy, pp.972-973, 2018

Cebi, A. H. Et Al. (2018) . "Whole exome sequencing helps the diagnosis of two siblings with SLC19A3 mutation." 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) , Milan, Italy, pp.972-973.

@conferencepaper{conferencepaper, author={ALPER HAN ÇEBİ Et Al. }, title={Whole exome sequencing helps the diagnosis of two siblings with SLC19A3 mutation}, congress name={51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG)}, city={Milan}, country={Italy}, year={2018}, pages={972-973} }