DOI: 10.1055/s-00029027

Journal of Pediatric Genetics

References

Mutlu-Albayrak H, Karaer K.
Vocal cord immobility as a cause of aphonia in a child with 3p13p12 deletion syndrome encompassing FOXP1 gene.

Int J Pediatr Otorhinolaryngol 2019;
117: 179-181

Download Bibliographical Data

Access:
Access: