APA

Lowther C., Speevak M., Armour C. M., Goh E. S., Graham G. E., Li C., Zeesman S., Nowaczyk M. J. M., Schultz L., Morra A., Nicolson R., Bikangaga P., Samdup D., Zaazou M., Boyd K., Jung J. H., Siu V., Rajguru M., Goobie S., Tarnopolsky M. A., Prasad C., Dick P. T., Hussain A. S., Walinga M., Reijenga R. G., Gazzellone M., Lionel A. C., Marshall C. R., Scherer S. W., Stavropoulos D. J., McCready E. & Bassett A. S. (20171207). Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression. : Genetics in medicine : official journal of the American College of Medical Genetics.

Chicago

Lowther Chelsea, Speevak Marsha, Armour Christine M, Goh Elaine S, Graham Gail E, Li Chumei, Zeesman Susan, Nowaczyk Malgorzata J M, Schultz Lee-Anne, Morra Antonella, Nicolson Rob, Bikangaga Peter, Samdup Dawa, Zaazou Mostafa, Boyd Kerry, Jung Jack H, Siu Victoria, Rajguru Manjulata, Goobie Sharan, Tarnopolsky Mark A, Prasad Chitra, Dick Paul T, Hussain Asmaa S, Walinga Margreet, Reijenga Renske G, Gazzellone Matthew, Lionel Anath C, Marshall Christian R, Scherer Stephen W, Stavropoulos Dimitri J, McCready Elizabeth and Bassett Anne S. 20171207. Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression. : Genetics in medicine : official journal of the American College of Medical Genetics.

Harvard

Lowther C., Speevak M., Armour C. M., Goh E. S., Graham G. E., Li C., Zeesman S., Nowaczyk M. J. M., Schultz L., Morra A., Nicolson R., Bikangaga P., Samdup D., Zaazou M., Boyd K., Jung J. H., Siu V., Rajguru M., Goobie S., Tarnopolsky M. A., Prasad C., Dick P. T., Hussain A. S., Walinga M., Reijenga R. G., Gazzellone M., Lionel A. C., Marshall C. R., Scherer S. W., Stavropoulos D. J., McCready E. and Bassett A. S. (20171207). Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression. : Genetics in medicine : official journal of the American College of Medical Genetics.

MLA

Lowther Chelsea, Speevak Marsha, Armour Christine M, Goh Elaine S, Graham Gail E, Li Chumei, Zeesman Susan, Nowaczyk Malgorzata J M, Schultz Lee-Anne, Morra Antonella, Nicolson Rob, Bikangaga Peter, Samdup Dawa, Zaazou Mostafa, Boyd Kerry, Jung Jack H, Siu Victoria, Rajguru Manjulata, Goobie Sharan, Tarnopolsky Mark A, Prasad Chitra, Dick Paul T, Hussain Asmaa S, Walinga Margreet, Reijenga Renske G, Gazzellone Matthew, Lionel Anath C, Marshall Christian R, Scherer Stephen W, Stavropoulos Dimitri J, McCready Elizabeth and Bassett Anne S. Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression. : Genetics in medicine : official journal of the American College of Medical Genetics. 20171207.