FGF3 gene mutations related to two syndromic Congenital deafness cases: Congenital deafness with inner ear agenesis (Michel aplasia), microtia, and microdontia and Otodental dysplasia


Turkyilmaz A., GEÇKİNLİ B. B. , Ates E. A. , SÖYLEMEZ M. A. , GÜNEY A. İ. , ATA P. , ...More

51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 16 - 19 June 2018, vol.27, pp.893 identifier

  • Publication Type: Conference Paper / Summary Text
  • Volume: 27
  • City: Milan
  • Country: Italy
  • Page Numbers: pp.893