Absence of major eye malformations further expands the phenotype of SOX2 deletions | AVESİS

Hacettepe University Research Information System

Absence of major eye malformations further expands the phenotype of SOX2 deletions

Copy For Citation

Guleray N., Demir G. U., Dogan O. A., Kiper P. O. S., Utine G. E., Alikasifoglu M.

50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.500-501, (Summary Text)

Publication Type: Conference Paper / Summary Text
Volume: 26
City: Copenhagen
Country: Denmark
Page Numbers: pp.500-501
Hacettepe University Affiliated: Yes