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


Guleray N., Demir G. U. , DOĞAN Ö. , Kiper P. O. S. , ÜTİNE G. E. , ALİKAŞİFOĞLU 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