Karamık, G. Et Al. 2022. Turnpenny Fry Syndrome: Clinical Report of a4 year old female with mutations in the PCGF2 gene. ESHG , (Vienna, Austria), 1439.

Karamık, G., Öztürk, N., Randa, N. C., Nur, B., & Mıhçı, E., (2022). Turnpenny Fry Syndrome: Clinical Report of a4 year old female with mutations in the PCGF2 gene . ESHG (pp.1439). Vienna, Austria

Karamık, GÖKCEN Et Al. "Turnpenny Fry Syndrome: Clinical Report of a4 year old female with mutations in the PCGF2 gene," ESHG, Vienna, Austria, 2022

Karamık, GÖKCEN Et Al. "Turnpenny Fry Syndrome: Clinical Report of a4 year old female with mutations in the PCGF2 gene." ESHG , Vienna, Austria, pp.1439, 2022

Karamık, G. Et Al. (2022) . "Turnpenny Fry Syndrome: Clinical Report of a4 year old female with mutations in the PCGF2 gene." ESHG , Vienna, Austria, p.1439.

@conferencepaper{conferencepaper, author={GÖKCEN KARAMIK Et Al. }, title={Turnpenny Fry Syndrome: Clinical Report of a4 year old female with mutations in the PCGF2 gene}, congress name={ESHG}, city={Vienna}, country={Austria}, year={2022}, pages={1439} }