GERİK ÇELEBİ, H. B. Et Al. 2017. A rare genetic syndrome with a new splice mutation detected in the EFTUD2 gene mandibulofacial disostosis, guion-almeida type.. European Human Genetics Conference .

GERİK ÇELEBİ, H. B., CEYLANER, S., & ÇAM, F. S., (2017). A rare genetic syndrome with a new splice mutation detected in the EFTUD2 gene mandibulofacial disostosis, guion-almeida type. . European Human Genetics Conference

GERİK ÇELEBİ, HAMİDE, SERDAR CEYLANER, And FETHİ SIRRI ÇAM. "A rare genetic syndrome with a new splice mutation detected in the EFTUD2 gene mandibulofacial disostosis, guion-almeida type.," European Human Genetics Conference, 2017

GERİK ÇELEBİ, HAMİDE B. Et Al. "A rare genetic syndrome with a new splice mutation detected in the EFTUD2 gene mandibulofacial disostosis, guion-almeida type.." European Human Genetics Conference , 2017

GERİK ÇELEBİ, H. B. CEYLANER, S. And ÇAM, F. S. (2017) . "A rare genetic syndrome with a new splice mutation detected in the EFTUD2 gene mandibulofacial disostosis, guion-almeida type.." European Human Genetics Conference .

@conferencepaper{conferencepaper, author={HAMİDE BETÜL GERİK ÇELEBİ Et Al. }, title={A rare genetic syndrome with a new splice mutation detected in the EFTUD2 gene mandibulofacial disostosis, guion-almeida type.}, congress name={European Human Genetics Conference}, city={}, country={}, year={2017}}