APA
van den Akker W. M. R., Brummelman I., Martis L. M., Timmermans R. N., Pfundt R., Kleefstra T., Willemsen M. H., Gerkes E. H., Herkert J. C., van Essen A. J., Rump P., Vansenne F., Terhal P. A., van Haelst M. M., Cristian I., Turner C. E., Cho M. T., Begtrup A., Willaert R., Fassi E., van Gassen K. L. I., Stegmann A. P. A., de Vries B. B. A. & Schuurs-Hoeijmakers J. H. M. (20190925). De novo variants in CDK13 associated with syndromic ID/DD: Molecular and clinical delineation of 15 individuals and a further review. : Clinical genetics.
Chicago
van den Akker W M R, Brummelman I, Martis L M, Timmermans R N, Pfundt R, Kleefstra T, Willemsen M H, Gerkes E H, Herkert J C, van Essen A J, Rump P, Vansenne F, Terhal P A, van Haelst M M, Cristian I, Turner C E, Cho M T, Begtrup A, Willaert R, Fassi E, van Gassen K L I, Stegmann A P A, de Vries B B A and Schuurs-Hoeijmakers J H M. 20190925. De novo variants in CDK13 associated with syndromic ID/DD: Molecular and clinical delineation of 15 individuals and a further review. : Clinical genetics.
Harvard
van den Akker W. M. R., Brummelman I., Martis L. M., Timmermans R. N., Pfundt R., Kleefstra T., Willemsen M. H., Gerkes E. H., Herkert J. C., van Essen A. J., Rump P., Vansenne F., Terhal P. A., van Haelst M. M., Cristian I., Turner C. E., Cho M. T., Begtrup A., Willaert R., Fassi E., van Gassen K. L. I., Stegmann A. P. A., de Vries B. B. A. and Schuurs-Hoeijmakers J. H. M. (20190925). De novo variants in CDK13 associated with syndromic ID/DD: Molecular and clinical delineation of 15 individuals and a further review. : Clinical genetics.
MLA
van den Akker W M R, Brummelman I, Martis L M, Timmermans R N, Pfundt R, Kleefstra T, Willemsen M H, Gerkes E H, Herkert J C, van Essen A J, Rump P, Vansenne F, Terhal P A, van Haelst M M, Cristian I, Turner C E, Cho M T, Begtrup A, Willaert R, Fassi E, van Gassen K L I, Stegmann A P A, de Vries B B A and Schuurs-Hoeijmakers J H M. De novo variants in CDK13 associated with syndromic ID/DD: Molecular and clinical delineation of 15 individuals and a further review. : Clinical genetics. 20190925.