APA

Kleefstra T., Brunner H. G., Amiel J., Oudakker A. R., Nillesen W. M., Magee A., Geneviève D., Cormier-Daire V., van Esch H., Fryns J., Hamel B. C. J., Sistermans E. A., de Vries B. B. A. & van Bokhoven H. (20060914). Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome. : American journal of human genetics.

Chicago

Kleefstra Tjitske, Brunner Han G, Amiel Jeanne, Oudakker Astrid R, Nillesen Willy M, Magee Alex, Geneviève David, Cormier-Daire Valérie, van Esch Hilde, Fryns Jean-Pierre, Hamel Ben C J, Sistermans Erik A, de Vries Bert B A and van Bokhoven Hans. 20060914. Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome. : American journal of human genetics.

Harvard

Kleefstra T., Brunner H. G., Amiel J., Oudakker A. R., Nillesen W. M., Magee A., Geneviève D., Cormier-Daire V., van Esch H., Fryns J., Hamel B. C. J., Sistermans E. A., de Vries B. B. A. and van Bokhoven H. (20060914). Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome. : American journal of human genetics.

MLA

Kleefstra Tjitske, Brunner Han G, Amiel Jeanne, Oudakker Astrid R, Nillesen Willy M, Magee Alex, Geneviève David, Cormier-Daire Valérie, van Esch Hilde, Fryns Jean-Pierre, Hamel Ben C J, Sistermans Erik A, de Vries Bert B A and van Bokhoven Hans. Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome. : American journal of human genetics. 20060914.