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 identifier

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