ERZURUMLUOĞLU GÖKALP, E. Et Al. 2017. De novo 7q31 deletion involving FOXP2 gene associated with speech disability. MOLECULAR CYTOGENETICS , vol.10 .

ERZURUMLUOĞLU GÖKALP, E., Ozdemir, M., Kocagil, S., ÇİLİNGİR, O., Tosumoglu, E., DURAK ARAS, B., ... ARTAN, S.(2017). De novo 7q31 deletion involving FOXP2 gene associated with speech disability. MOLECULAR CYTOGENETICS , vol.10.

ERZURUMLUOĞLU GÖKALP, EBRU Et Al. "De novo 7q31 deletion involving FOXP2 gene associated with speech disability," MOLECULAR CYTOGENETICS , vol.10, 2017

ERZURUMLUOĞLU GÖKALP, EBRU E. Et Al. "De novo 7q31 deletion involving FOXP2 gene associated with speech disability." MOLECULAR CYTOGENETICS , vol.10, 2017

ERZURUMLUOĞLU GÖKALP, E. Et Al. (2017) . "De novo 7q31 deletion involving FOXP2 gene associated with speech disability." MOLECULAR CYTOGENETICS , vol.10.

@article{article, author={EBRU ERZURUMLUOĞLU GÖKALP Et Al. }, title={De novo 7q31 deletion involving FOXP2 gene associated with speech disability}, journal={MOLECULAR CYTOGENETICS}, year=2017}