APA

Beunders G., de Munnik S. A., Van der Aa N., Ceulemans B., Voorhoeve E., Groffen A. J., Nillesen W. M., Meijers-Heijboer E. J., Frank Kooy R., Yntema H. G. & Sistermans E. A. (20160203). Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndrome. : European journal of human genetics : EJHG.

Chicago

Beunders Gea, de Munnik Sonja A, Van der Aa Nathalie, Ceulemans Berten, Voorhoeve Els, Groffen Alexander J, Nillesen Willy M, Meijers-Heijboer Elizabeth J, Frank Kooy R, Yntema Helger G and Sistermans Erik A. 20160203. Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndrome. : European journal of human genetics : EJHG.

Harvard

Beunders G., de Munnik S. A., Van der Aa N., Ceulemans B., Voorhoeve E., Groffen A. J., Nillesen W. M., Meijers-Heijboer E. J., Frank Kooy R., Yntema H. G. and Sistermans E. A. (20160203). Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndrome. : European journal of human genetics : EJHG.

MLA

Beunders Gea, de Munnik Sonja A, Van der Aa Nathalie, Ceulemans Berten, Voorhoeve Els, Groffen Alexander J, Nillesen Willy M, Meijers-Heijboer Elizabeth J, Frank Kooy R, Yntema Helger G and Sistermans Erik A. Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndrome. : European journal of human genetics : EJHG. 20160203.