APA
Shashi V., Pena L. D. M., Kim K., Burton B., Hempel M., Schoch K., Walkiewicz M., McLaughlin H. M., Cho M., Stong N., Hickey S. E., Shuss C. M., Freemark M. S., Bellet J. S., Keels M. A., Bonner M. J., El-Dairi M., Butler M., Kranz P. G., Stumpel C. T. R. M., Klinkenberg S., Oberndorff K., Alawi M., Santer R., Petrovski S., Kuismin O., Korpi-Heikkilä S., Pietilainen O., Aarno P., Kurki M. I., Hoischen A., Need A. C., Goldstein D. B. & Kortüm F. (012017). De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype. : American journal of human genetics.
Chicago
Shashi Vandana, Pena Loren D M, Kim Katherine, Burton Barbara, Hempel Maja, Schoch Kelly, Walkiewicz Magdalena, McLaughlin Heather M, Cho Megan, Stong Nicholas, Hickey Scott E, Shuss Christine M, Freemark Michael S, Bellet Jane S, Keels Martha Ann, Bonner Melanie J, El-Dairi Maysantoine, Butler Megan, Kranz Peter G, Stumpel Constance T R M, Klinkenberg Sylvia, Oberndorff Karin, Alawi Malik, Santer Rene, Petrovski Slavé, Kuismin Outi, Korpi-Heikkilä Satu, Pietilainen Olli, Aarno Palotie, Kurki Mitja I, Hoischen Alexander, Need Anna C, Goldstein David B and Kortüm Fanny. 012017. De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype. : American journal of human genetics.
Harvard
Shashi V., Pena L. D. M., Kim K., Burton B., Hempel M., Schoch K., Walkiewicz M., McLaughlin H. M., Cho M., Stong N., Hickey S. E., Shuss C. M., Freemark M. S., Bellet J. S., Keels M. A., Bonner M. J., El-Dairi M., Butler M., Kranz P. G., Stumpel C. T. R. M., Klinkenberg S., Oberndorff K., Alawi M., Santer R., Petrovski S., Kuismin O., Korpi-Heikkilä S., Pietilainen O., Aarno P., Kurki M. I., Hoischen A., Need A. C., Goldstein D. B. and Kortüm F. (012017). De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype. : American journal of human genetics.
MLA
Shashi Vandana, Pena Loren D M, Kim Katherine, Burton Barbara, Hempel Maja, Schoch Kelly, Walkiewicz Magdalena, McLaughlin Heather M, Cho Megan, Stong Nicholas, Hickey Scott E, Shuss Christine M, Freemark Michael S, Bellet Jane S, Keels Martha Ann, Bonner Melanie J, El-Dairi Maysantoine, Butler Megan, Kranz Peter G, Stumpel Constance T R M, Klinkenberg Sylvia, Oberndorff Karin, Alawi Malik, Santer Rene, Petrovski Slavé, Kuismin Outi, Korpi-Heikkilä Satu, Pietilainen Olli, Aarno Palotie, Kurki Mitja I, Hoischen Alexander, Need Anna C, Goldstein David B and Kortüm Fanny. De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype. : American journal of human genetics. 012017.