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

  • Publication Type: Conference Paper / Summary Text
  • Volume: 10
  • Doi Number: 10.1186/s13039-017-0319-3
  • Eskisehir Osmangazi University Affiliated: Yes