A rare genetic syndrome with a new splice mutation detected in the EFTUD2 gene mandibulofacial disostosis, guion-almeida type.

GERİK ÇELEBİ H. B., CEYLANER S., ÇAM F. S.

European Human Genetics Conference, 27 - 30 May 2017, (Summary Text)

  • Publication Type: Conference Paper / Summary Text
  • Manisa Celal Bayar University Affiliated: Yes