Ö. AKGÜN DOĞAN Et Al. , "Two new patients with acromesomelic dysplasia, PRKG2 type-identification and characterization of the first missense variant," EUROPEAN JOURNAL OF HUMAN GENETICS , 2023
AKGÜN DOĞAN, Ö. Et Al. 2023. Two new patients with acromesomelic dysplasia, PRKG2 type-identification and characterization of the first missense variant. EUROPEAN JOURNAL OF HUMAN GENETICS .
AKGÜN DOĞAN, Ö., Diaz-Gonzalez, F., de Lima Jorge, A. A., Onenli-Mungan, N., Menezes Andrade, N. L., de Polli Cellin, L., ... CEYLANER, S.(2023). Two new patients with acromesomelic dysplasia, PRKG2 type-identification and characterization of the first missense variant. EUROPEAN JOURNAL OF HUMAN GENETICS .
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 , 2023
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 , 2023
AKGÜN DOĞAN, Ö. Et Al. (2023) . "Two new patients with acromesomelic dysplasia, PRKG2 type-identification and characterization of the first missense variant." EUROPEAN JOURNAL OF HUMAN GENETICS .
@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=2023}