APA

Powis Z., Petrik I., Cohen J. S., Escolar D., Burton J., van Ravenswaaij-Arts C. M. A., Sival D. A., Stegmann A. P. A., Kleefstra T., Pfundt R., Chikarmane R., Begtrup A., Huether R., Tang S. & Shinde D. N. (20190925). De novo variants in KLF7 are a potential novel cause of developmental delay/intellectual disability, neuromuscular and psychiatric symptoms. : Clinical genetics.

Chicago

Powis Z, Petrik I, Cohen J S, Escolar D, Burton J, van Ravenswaaij-Arts C M A, Sival D A, Stegmann A P A, Kleefstra T, Pfundt R, Chikarmane R, Begtrup A, Huether R, Tang S and Shinde D N. 20190925. De novo variants in KLF7 are a potential novel cause of developmental delay/intellectual disability, neuromuscular and psychiatric symptoms. : Clinical genetics.

Harvard

Powis Z., Petrik I., Cohen J. S., Escolar D., Burton J., van Ravenswaaij-Arts C. M. A., Sival D. A., Stegmann A. P. A., Kleefstra T., Pfundt R., Chikarmane R., Begtrup A., Huether R., Tang S. and Shinde D. N. (20190925). De novo variants in KLF7 are a potential novel cause of developmental delay/intellectual disability, neuromuscular and psychiatric symptoms. : Clinical genetics.

MLA

Powis Z, Petrik I, Cohen J S, Escolar D, Burton J, van Ravenswaaij-Arts C M A, Sival D A, Stegmann A P A, Kleefstra T, Pfundt R, Chikarmane R, Begtrup A, Huether R, Tang S and Shinde D N. De novo variants in KLF7 are a potential novel cause of developmental delay/intellectual disability, neuromuscular and psychiatric symptoms. : Clinical genetics. 20190925.