APA
Chaudhry A., Noor A., Degagne B., Baker K., Bok L. A., Brady A. F., Chitayat D., Chung B. H., Cytrynbaum C., Dyment D., Filges I., Helm B., Hutchison H. T., Jeng L. J. B., Laumonnier F., Marshall C. R., Menzel M., Parkash S., Parker M. J., Raymond L. F., Rideout A. L., Roberts W., Rupps R., Schanze I., Schrander-Stumpel C. T. R. M., Speevak M. D., Stavropoulos D. J., Stevens S. J. C., Thomas E. R. A., Toutain A., Vergano S., Weksberg R., Scherer S. W., Vincent J. B. & Carter M. T. (20160510). Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorder. : Clinical genetics.
Chicago
Chaudhry A, Noor A, Degagne B, Baker K, Bok L A, Brady A F, Chitayat D, Chung B H, Cytrynbaum C, Dyment D, Filges I, Helm B, Hutchison H T, Jeng L J B, Laumonnier F, Marshall C R, Menzel M, Parkash S, Parker M J, Raymond L F, Rideout A L, Roberts W, Rupps R, Schanze I, Schrander-Stumpel C T R M, Speevak M D, Stavropoulos D J, Stevens S J C, Thomas E R A, Toutain A, Vergano S, Weksberg R, Scherer S W, Vincent J B and Carter M T. 20160510. Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorder. : Clinical genetics.
Harvard
Chaudhry A., Noor A., Degagne B., Baker K., Bok L. A., Brady A. F., Chitayat D., Chung B. H., Cytrynbaum C., Dyment D., Filges I., Helm B., Hutchison H. T., Jeng L. J. B., Laumonnier F., Marshall C. R., Menzel M., Parkash S., Parker M. J., Raymond L. F., Rideout A. L., Roberts W., Rupps R., Schanze I., Schrander-Stumpel C. T. R. M., Speevak M. D., Stavropoulos D. J., Stevens S. J. C., Thomas E. R. A., Toutain A., Vergano S., Weksberg R., Scherer S. W., Vincent J. B. and Carter M. T. (20160510). Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorder. : Clinical genetics.
MLA
Chaudhry A, Noor A, Degagne B, Baker K, Bok L A, Brady A F, Chitayat D, Chung B H, Cytrynbaum C, Dyment D, Filges I, Helm B, Hutchison H T, Jeng L J B, Laumonnier F, Marshall C R, Menzel M, Parkash S, Parker M J, Raymond L F, Rideout A L, Roberts W, Rupps R, Schanze I, Schrander-Stumpel C T R M, Speevak M D, Stavropoulos D J, Stevens S J C, Thomas E R A, Toutain A, Vergano S, Weksberg R, Scherer S W, Vincent J B and Carter M T. Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorder. : Clinical genetics. 20160510.