ERZURUMLUOĞLU, E. Et Al. 2017. De novo 7q31 deletion involving FOXP2 gene associated with speech disability. 11th European Cytogenetic Conference 2017 .

ERZURUMLUOĞLU, E., ÖZDEMİR, M., KOCAGİL, S., ÇİLİNGİR, O., TOSUMOĞLU, E., DURAK ARAS, B., ... ARTAN, S.(2017). De novo 7q31 deletion involving FOXP2 gene associated with speech disability . 11th European Cytogenetic Conference 2017

ERZURUMLUOĞLU, EBRU Et Al. "De novo 7q31 deletion involving FOXP2 gene associated with speech disability," 11th European Cytogenetic Conference 2017, 2017

ERZURUMLUOĞLU, EBRU E. Et Al. "De novo 7q31 deletion involving FOXP2 gene associated with speech disability." 11th European Cytogenetic Conference 2017 , 2017

ERZURUMLUOĞLU, E. Et Al. (2017) . "De novo 7q31 deletion involving FOXP2 gene associated with speech disability." 11th European Cytogenetic Conference 2017 .

@conferencepaper{conferencepaper, author={EBRU ERZURUMLUOĞLU GÖKALP Et Al. }, title={De novo 7q31 deletion involving FOXP2 gene associated with speech disability}, congress name={11th European Cytogenetic Conference 2017}, city={}, country={}, year={2017}}