H. Mutlu-Albayrak And K. Karaer, "Vocal cord immobility as a cause of aphonia in a child with 3p13p12 deletion syndrome encompassing FOXP1 gene," INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY , vol.117, pp.179-181, 2019
Mutlu-Albayrak, H. And Karaer, K. 2019. Vocal cord immobility as a cause of aphonia in a child with 3p13p12 deletion syndrome encompassing FOXP1 gene. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY , vol.117 , 179-181.
Mutlu-Albayrak, H., & Karaer, K., (2019). Vocal cord immobility as a cause of aphonia in a child with 3p13p12 deletion syndrome encompassing FOXP1 gene. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY , vol.117, 179-181.
Mutlu-Albayrak, HATİCE, And Kadri Karaer. "Vocal cord immobility as a cause of aphonia in a child with 3p13p12 deletion syndrome encompassing FOXP1 gene," INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY , vol.117, 179-181, 2019
Mutlu-Albayrak, HATİCE And Karaer, Kadri. "Vocal cord immobility as a cause of aphonia in a child with 3p13p12 deletion syndrome encompassing FOXP1 gene." INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY , vol.117, pp.179-181, 2019
Mutlu-Albayrak, H. And Karaer, K. (2019) . "Vocal cord immobility as a cause of aphonia in a child with 3p13p12 deletion syndrome encompassing FOXP1 gene." INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY , vol.117, pp.179-181.
@article{article, author={HATİCE MUTLU And author={Kadri Karaer}, title={Vocal cord immobility as a cause of aphonia in a child with 3p13p12 deletion syndrome encompassing FOXP1 gene}, journal={INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY}, year=2019, pages={179-181} }