APA
Nabais Sá M. J., Jensik P. J., McGee S. R., Parker M. J., Lahiri N., McNeil E. P., Kroes H. Y., Hagerman R. J., Harrison R. E., Montgomery T., Splitt M., Palmer E. E., Sachdev R. K., Mefford H. C., Scott A. A., Martinez-Agosto J. A., Lorenz R., Orenstein N., Berg J. N., Amiel J., Heron D., Keren B., Cobben J., Menke L. A., Marco E. J., Graham J. M., Pierson T. M., Karimiani E. G., Maroofian R., Manzini M. C., Cauley E. S., Colombo R., Odent S., Dubourg C., Phornphutkul C., de Brouwer A. P. M., de Vries B. B. A. & Vulto-vanSilfhout A. T. (20200204). De novo and biallelic DEAF1 variants cause a phenotypic spectrum. : Genetics in medicine : official journal of the American College of Medical Genetics.
Chicago
Nabais Sá Maria J, Jensik Philip J, McGee Stacey R, Parker Michael J, Lahiri Nayana, McNeil Evan P, Kroes Hester Y, Hagerman Randi J, Harrison Rachel E, Montgomery Tara, Splitt Miranda, Palmer Elizabeth E, Sachdev Rani K, Mefford Heather C, Scott Abbey A, Martinez-Agosto Julian A, Lorenz Rüdiger, Orenstein Naama, Berg Jonathan N, Amiel Jeanne, Heron Delphine, Keren Boris, Cobben Jan-Maarten, Menke Leonie A, Marco Elysa J, Graham John M, Pierson Tyler Mark, Karimiani Ehsan Ghayoor, Maroofian Reza, Manzini M Chiara, Cauley Edmund S, Colombo Roberto, Odent Sylvie, Dubourg Christele, Phornphutkul Chanika, de Brouwer Arjan P M, de Vries Bert B A and Vulto-vanSilfhout Anneke T. 20200204. De novo and biallelic DEAF1 variants cause a phenotypic spectrum. : Genetics in medicine : official journal of the American College of Medical Genetics.
Harvard
Nabais Sá M. J., Jensik P. J., McGee S. R., Parker M. J., Lahiri N., McNeil E. P., Kroes H. Y., Hagerman R. J., Harrison R. E., Montgomery T., Splitt M., Palmer E. E., Sachdev R. K., Mefford H. C., Scott A. A., Martinez-Agosto J. A., Lorenz R., Orenstein N., Berg J. N., Amiel J., Heron D., Keren B., Cobben J., Menke L. A., Marco E. J., Graham J. M., Pierson T. M., Karimiani E. G., Maroofian R., Manzini M. C., Cauley E. S., Colombo R., Odent S., Dubourg C., Phornphutkul C., de Brouwer A. P. M., de Vries B. B. A. and Vulto-vanSilfhout A. T. (20200204). De novo and biallelic DEAF1 variants cause a phenotypic spectrum. : Genetics in medicine : official journal of the American College of Medical Genetics.
MLA
Nabais Sá Maria J, Jensik Philip J, McGee Stacey R, Parker Michael J, Lahiri Nayana, McNeil Evan P, Kroes Hester Y, Hagerman Randi J, Harrison Rachel E, Montgomery Tara, Splitt Miranda, Palmer Elizabeth E, Sachdev Rani K, Mefford Heather C, Scott Abbey A, Martinez-Agosto Julian A, Lorenz Rüdiger, Orenstein Naama, Berg Jonathan N, Amiel Jeanne, Heron Delphine, Keren Boris, Cobben Jan-Maarten, Menke Leonie A, Marco Elysa J, Graham John M, Pierson Tyler Mark, Karimiani Ehsan Ghayoor, Maroofian Reza, Manzini M Chiara, Cauley Edmund S, Colombo Roberto, Odent Sylvie, Dubourg Christele, Phornphutkul Chanika, de Brouwer Arjan P M, de Vries Bert B A and Vulto-vanSilfhout Anneke T. De novo and biallelic DEAF1 variants cause a phenotypic spectrum. : Genetics in medicine : official journal of the American College of Medical Genetics. 20200204.