De novo 7q31 deletion involving FOXP2 gene associated with speech disability


ERZURUMLUOĞLU E. , ÖZDEMİR M., KOCAGİL S. , ÇİLİNGİR O. , TOSUMOĞLU E., DURAK ARAS B. , ...More

11th European Cytogenetic Conference 2017, 1 - 04 July 2017, vol.10