Tuncel, G. Et Al. 2021. Identification of a Novel De Novo COMP Gene Variant as a Likely Cause of Pseudoachondroplasia. APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY , vol.29, no.7 , 546-550.

Tuncel, G., Akcan, N., Gul, Ş., Sag, S. O., Bundak, R., Mocan, G., ... TEMEL, Ş. G.(2021). Identification of a Novel De Novo COMP Gene Variant as a Likely Cause of Pseudoachondroplasia. APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY , vol.29, no.7, 546-550.

Tuncel, Gulten Et Al. "Identification of a Novel De Novo COMP Gene Variant as a Likely Cause of Pseudoachondroplasia," APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY , vol.29, no.7, 546-550, 2021

Tuncel, Gulten Et Al. "Identification of a Novel De Novo COMP Gene Variant as a Likely Cause of Pseudoachondroplasia." APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY , vol.29, no.7, pp.546-550, 2021

Tuncel, G. Et Al. (2021) . "Identification of a Novel De Novo COMP Gene Variant as a Likely Cause of Pseudoachondroplasia." APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY , vol.29, no.7, pp.546-550.

@article{article, author={Gulten Tuncel Et Al. }, title={Identification of a Novel De Novo COMP Gene Variant as a Likely Cause of Pseudoachondroplasia}, journal={APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY}, year=2021, pages={546-550} }