APA ציטוט

Massink, M., Créton, M., Spanevello, F., Fennis, W., Cune, M., Savelberg, S., . . . van Haaften, G. (2015). Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia. Am J Hum Genet.

Citação norma Chicago

Massink, Maarten P.G., et al. "Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia." Am J Hum Genet 2015.

ציטוט MLA

Massink, Maarten P.G., et al. "Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia." Am J Hum Genet 2015.