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


TÜRKYILMAZ A., GEÇKİNLİ B. B., ARSLAN ATEŞ E., SÖYLEMEZ M. A., GÜNEY A. İ., ATA P., ...More

51st European Society of Human Genetics Conference, Milan, Italy, 16 June 2018, vol.27, pp.893

  • Publication Type: Conference Paper / Summary Text
  • Volume: 27
  • Doi Number: 10.1038/s41431-019-0408-3
  • City: Milan
  • Country: Italy
  • Page Numbers: pp.893
  • Karadeniz Technical University Affiliated: No