APA

Repnikova E. A., Lyalin D. A., McDonald K., Astbury C., Hansen-Kiss E., Cooley L. D., Pfau R., Herman G. E., Pyatt R. E. & Hickey S. E. (20200930). CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders. : European journal of medical genetics.

Chicago

Repnikova Elena A, Lyalin Dmitry A, McDonald Kimberly, Astbury Caroline, Hansen-Kiss Emily, Cooley Linda D, Pfau Ruthann, Herman Gail E, Pyatt Robert E and Hickey Scott E. 20200930. CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders. : European journal of medical genetics.

Harvard

Repnikova E. A., Lyalin D. A., McDonald K., Astbury C., Hansen-Kiss E., Cooley L. D., Pfau R., Herman G. E., Pyatt R. E. and Hickey S. E. (20200930). CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders. : European journal of medical genetics.

MLA

Repnikova Elena A, Lyalin Dmitry A, McDonald Kimberly, Astbury Caroline, Hansen-Kiss Emily, Cooley Linda D, Pfau Ruthann, Herman Gail E, Pyatt Robert E and Hickey Scott E. CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders. : European journal of medical genetics. 20200930.