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


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) identifier

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