Tuncel, G. Et Al. 2021. A Homozygous Synonymous Variant Likely Cause of Severe Ciliopathy Phenotype. GENES , vol.12, no.6 .

Tuncel, G., Kaymakamzade, B., Engindereli, Y., TEMEL, Ş. G., & Ergoren, M. C., (2021). A Homozygous Synonymous Variant Likely Cause of Severe Ciliopathy Phenotype. GENES , vol.12, no.6.

Tuncel, Gulten Et Al. "A Homozygous Synonymous Variant Likely Cause of Severe Ciliopathy Phenotype," GENES , vol.12, no.6, 2021

Tuncel, Gulten Et Al. "A Homozygous Synonymous Variant Likely Cause of Severe Ciliopathy Phenotype." GENES , vol.12, no.6, 2021

Tuncel, G. Et Al. (2021) . "A Homozygous Synonymous Variant Likely Cause of Severe Ciliopathy Phenotype." GENES , vol.12, no.6.

@article{article, author={Gulten Tuncel Et Al. }, title={A Homozygous Synonymous Variant Likely Cause of Severe Ciliopathy Phenotype}, journal={GENES}, year=2021}