Guleray, N. Et Al. 2017. Absence of major eye malformations further expands the phenotype of SOX2 deletions. 50th European-Society-of-Human-Genetics (ESHG) Conference , (Copenhagen, Denmark), 500-501.

Guleray, N., Demir, G. U., Dogan, O. A., Kiper, P. O. S., Utine, G. E., & Alikasifoglu, M., (2017). Absence of major eye malformations further expands the phenotype of SOX2 deletions . 50th European-Society-of-Human-Genetics (ESHG) Conference (pp.500-501). Copenhagen, Denmark

Guleray, N. Et Al. "Absence of major eye malformations further expands the phenotype of SOX2 deletions," 50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 2017

Guleray, N. Et Al. "Absence of major eye malformations further expands the phenotype of SOX2 deletions." 50th European-Society-of-Human-Genetics (ESHG) Conference , Copenhagen, Denmark, pp.500-501, 2017

Guleray, N. Et Al. (2017) . "Absence of major eye malformations further expands the phenotype of SOX2 deletions." 50th European-Society-of-Human-Genetics (ESHG) Conference , Copenhagen, Denmark, pp.500-501.

@conferencepaper{conferencepaper, author={N. Guleray Et Al. }, title={Absence of major eye malformations further expands the phenotype of SOX2 deletions}, congress name={50th European-Society-of-Human-Genetics (ESHG) Conference}, city={Copenhagen}, country={Denmark}, year={2017}, pages={500-501} }