APA
McEntagart M., Williamson K. A., Rainger J. K., Wheeler A., Seawright A., De Baere E., Verdin H., Bergendahl L. T., Quigley A., Rainger J., Dixit A., Sarkar A., López Laso E., Sanchez-Carpintero R., Barrio J., Bitoun P., Prescott T., Riise R., McKee S., Cook J., McKie L., Ceulemans B., Meire F., Temple I. K., Prieur F., Williams J., Clouston P., Németh A. H., Banka S., Bengani H., Handley M., Freyer E., Ross A., van Heyningen V., Marsh J. A., Elmslie F. & FitzPatrick D. R. (20170515). A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative Effect. : American journal of human genetics.
Chicago
McEntagart Meriel, Williamson Kathleen A, Rainger Jacqueline K, Wheeler Ann, Seawright Anne, De Baere Elfride, Verdin Hannah, Bergendahl L Therese, Quigley Alan, Rainger Joe, Dixit Abhijit, Sarkar Ajoy, López Laso Eduardo, Sanchez-Carpintero Rocio, Barrio Jesus, Bitoun Pierre, Prescott Trine, Riise Ruth, McKee Shane, Cook Jackie, McKie Lisa, Ceulemans Berten, Meire Françoise, Temple I Karen, Prieur Fabienne, Williams Jonathan, Clouston Penny, Németh Andrea H, Banka Siddharth, Bengani Hemant, Handley Mark, Freyer Elisabeth, Ross Allyson, van Heyningen Veronica, Marsh Joseph A, Elmslie Frances and FitzPatrick David R. 20170515. A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative Effect. : American journal of human genetics.
Harvard
McEntagart M., Williamson K. A., Rainger J. K., Wheeler A., Seawright A., De Baere E., Verdin H., Bergendahl L. T., Quigley A., Rainger J., Dixit A., Sarkar A., López Laso E., Sanchez-Carpintero R., Barrio J., Bitoun P., Prescott T., Riise R., McKee S., Cook J., McKie L., Ceulemans B., Meire F., Temple I. K., Prieur F., Williams J., Clouston P., Németh A. H., Banka S., Bengani H., Handley M., Freyer E., Ross A., van Heyningen V., Marsh J. A., Elmslie F. and FitzPatrick D. R. (20170515). A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative Effect. : American journal of human genetics.
MLA
McEntagart Meriel, Williamson Kathleen A, Rainger Jacqueline K, Wheeler Ann, Seawright Anne, De Baere Elfride, Verdin Hannah, Bergendahl L Therese, Quigley Alan, Rainger Joe, Dixit Abhijit, Sarkar Ajoy, López Laso Eduardo, Sanchez-Carpintero Rocio, Barrio Jesus, Bitoun Pierre, Prescott Trine, Riise Ruth, McKee Shane, Cook Jackie, McKie Lisa, Ceulemans Berten, Meire Françoise, Temple I Karen, Prieur Fabienne, Williams Jonathan, Clouston Penny, Németh Andrea H, Banka Siddharth, Bengani Hemant, Handley Mark, Freyer Elisabeth, Ross Allyson, van Heyningen Veronica, Marsh Joseph A, Elmslie Frances and FitzPatrick David R. A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative Effect. : American journal of human genetics. 20170515.