APA
Bijlsma E. K., Gijsbers A. C. J., Schuurs-Hoeijmakers J. H. M., van Haeringen A., Fransen van de Putte D. E., Anderlid B., Lundin J., Lapunzina P., Pérez Jurado L. A., Delle Chiaie B., Loeys B., Menten B., Oostra A., Verhelst H., Amor D. J., Bruno D. L., van Essen A. J., Hordijk R., Sikkema-Raddatz B., Verbruggen K. T., Jongmans M. C. J., Pfundt R., Reeser H. M., Breuning M. H. & Ruivenkamp C. A. L. (20090901). Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals. : European journal of medical genetics.
Chicago
Bijlsma E K, Gijsbers A C J, Schuurs-Hoeijmakers J H M, van Haeringen A, Fransen van de Putte D E, Anderlid B-M, Lundin J, Lapunzina P, Pérez Jurado L A, Delle Chiaie B, Loeys B, Menten B, Oostra A, Verhelst H, Amor D J, Bruno D L, van Essen A J, Hordijk R, Sikkema-Raddatz B, Verbruggen K T, Jongmans M C J, Pfundt R, Reeser H M, Breuning M H and Ruivenkamp C A L. 20090901. Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals. : European journal of medical genetics.
Harvard
Bijlsma E. K., Gijsbers A. C. J., Schuurs-Hoeijmakers J. H. M., van Haeringen A., Fransen van de Putte D. E., Anderlid B., Lundin J., Lapunzina P., Pérez Jurado L. A., Delle Chiaie B., Loeys B., Menten B., Oostra A., Verhelst H., Amor D. J., Bruno D. L., van Essen A. J., Hordijk R., Sikkema-Raddatz B., Verbruggen K. T., Jongmans M. C. J., Pfundt R., Reeser H. M., Breuning M. H. and Ruivenkamp C. A. L. (20090901). Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals. : European journal of medical genetics.
MLA
Bijlsma E K, Gijsbers A C J, Schuurs-Hoeijmakers J H M, van Haeringen A, Fransen van de Putte D E, Anderlid B-M, Lundin J, Lapunzina P, Pérez Jurado L A, Delle Chiaie B, Loeys B, Menten B, Oostra A, Verhelst H, Amor D J, Bruno D L, van Essen A J, Hordijk R, Sikkema-Raddatz B, Verbruggen K T, Jongmans M C J, Pfundt R, Reeser H M, Breuning M H and Ruivenkamp C A L. Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals. : European journal of medical genetics. 20090901.