APA

Vissers L. E. L. M., Bonetti M., Paardekooper Overman J., Nillesen W. M., Frints S. G. M., de Ligt J., Zampino G., Justino A., Machado J. C., Schepens M., Brunner H. G., Veltman J. A., Scheffer H., Gros P., Costa J. L., Tartaglia M., van der Burgt I., Yntema H. G. & den Hertog J. (20151022). Heterozygous germline mutations in A2ML1 are associated with a disorder clinically related to Noonan syndrome. : European journal of human genetics : EJHG.

Chicago

Vissers Lisenka E L M, Bonetti Monica, Paardekooper Overman Jeroen, Nillesen Willy M, Frints Suzanna G M, de Ligt Joep, Zampino Giuseppe, Justino Ana, Machado José C, Schepens Marga, Brunner Han G, Veltman Joris A, Scheffer Hans, Gros Piet, Costa José L, Tartaglia Marco, van der Burgt Ineke, Yntema Helger G and den Hertog Jeroen. 20151022. Heterozygous germline mutations in A2ML1 are associated with a disorder clinically related to Noonan syndrome. : European journal of human genetics : EJHG.

Harvard

Vissers L. E. L. M., Bonetti M., Paardekooper Overman J., Nillesen W. M., Frints S. G. M., de Ligt J., Zampino G., Justino A., Machado J. C., Schepens M., Brunner H. G., Veltman J. A., Scheffer H., Gros P., Costa J. L., Tartaglia M., van der Burgt I., Yntema H. G. and den Hertog J. (20151022). Heterozygous germline mutations in A2ML1 are associated with a disorder clinically related to Noonan syndrome. : European journal of human genetics : EJHG.

MLA

Vissers Lisenka E L M, Bonetti Monica, Paardekooper Overman Jeroen, Nillesen Willy M, Frints Suzanna G M, de Ligt Joep, Zampino Giuseppe, Justino Ana, Machado José C, Schepens Marga, Brunner Han G, Veltman Joris A, Scheffer Hans, Gros Piet, Costa José L, Tartaglia Marco, van der Burgt Ineke, Yntema Helger G and den Hertog Jeroen. Heterozygous germline mutations in A2ML1 are associated with a disorder clinically related to Noonan syndrome. : European journal of human genetics : EJHG. 20151022.