Motta, M. Et Al. 2021. SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype. AMERICAN JOURNAL OF HUMAN GENETICS , vol.108, no.11 , 2112-2129.

Motta, M., Fasano, G., Gredy, S., Brinkmann, J., Bonnard, A. A., ŞİMŞEK KİPER, P. Ö., ... Gulec, E. Y.(2021). SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype. AMERICAN JOURNAL OF HUMAN GENETICS , vol.108, no.11, 2112-2129.

Motta, Marialetizia Et Al. "SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype," AMERICAN JOURNAL OF HUMAN GENETICS , vol.108, no.11, 2112-2129, 2021

Motta, Marialetizia Et Al. "SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype." AMERICAN JOURNAL OF HUMAN GENETICS , vol.108, no.11, pp.2112-2129, 2021

Motta, M. Et Al. (2021) . "SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype." AMERICAN JOURNAL OF HUMAN GENETICS , vol.108, no.11, pp.2112-2129.

@article{article, author={Marialetizia Motta Et Al. }, title={SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype}, journal={AMERICAN JOURNAL OF HUMAN GENETICS}, year=2021, pages={2112-2129} }