AKGÜN DOĞAN, Ö. Et Al. 2024. Two new patients with acromesomelic dysplasia, PRKG2 type—identification and characterization of the first missense variant. European Journal of Human Genetics , vol.32, no.10 , 1250-1256.

AKGÜN DOĞAN, Ö., Díaz-González, F., de Lima Jorge, A. A., Onenli-Mungan, N., Menezes Andrade, N. L., de Polli Cellin, L., ... CEYLANER, S.(2024). Two new patients with acromesomelic dysplasia, PRKG2 type—identification and characterization of the first missense variant. European Journal of Human Genetics , vol.32, no.10, 1250-1256.

AKGÜN DOĞAN, ÖZLEM Et Al. "Two new patients with acromesomelic dysplasia, PRKG2 type—identification and characterization of the first missense variant," European Journal of Human Genetics , vol.32, no.10, 1250-1256, 2024

AKGÜN DOĞAN, ÖZLEM A. Et Al. "Two new patients with acromesomelic dysplasia, PRKG2 type—identification and characterization of the first missense variant." European Journal of Human Genetics , vol.32, no.10, pp.1250-1256, 2024

AKGÜN DOĞAN, Ö. Et Al. (2024) . "Two new patients with acromesomelic dysplasia, PRKG2 type—identification and characterization of the first missense variant." European Journal of Human Genetics , vol.32, no.10, pp.1250-1256.

@article{article, author={ÖZLEM AKGÜN DOĞAN Et Al. }, title={Two new patients with acromesomelic dysplasia, PRKG2 type—identification and characterization of the first missense variant}, journal={European Journal of Human Genetics}, year=2024, pages={1250-1256} }