APA Citation

Burrage, L., Charng, W., Eldomery, M., Willer, J., Davis, E., Lugtenberg, D., . . . Yang, Y. (2015). De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. Am J Hum Genet.

Citação norma Chicago

Burrage, Lindsay C., et al. "De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated With Meier-Gorlin Syndrome." Am J Hum Genet 2015.

MLA Citation

Burrage, Lindsay C., et al. "De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated With Meier-Gorlin Syndrome." Am J Hum Genet 2015.

Advarsel: Disse citationer er muligvist ikke 100% nøjagtige.