APA
Fountain M. D., Oleson D. S., Rech M. E., Segebrecht L., Hunter J. V., McCarthy J. M., Lupo P. J., Holtgrewe M., Moran R., Rosenfeld J. A., Isidor B., Le Caignec C., Saenz M. S., Pedersen R. C., Morgan T. M., Pfotenhauer J. P., Xia F., Bi W., Kang S. L., Patel A., Krantz I. D., Raible S. E., Smith W., Cristian I., Torti E., Juusola J., Millan F., Wentzensen I. M., Person R. E., Küry S., Bézieau S., Uguen K., Férec C., Munnich A., van Haelst M., Lichtenbelt K. D., van Gassen K., Hagelstrom T., Chawla A., Perry D. L., Taft R. J., Jones M., Masser-Frye D., Dyment D., Venkateswaran S., Li C., Escobar L. F., Horn D., Spillmann R. C., Peña L., Wierzba J., Strom T. M., Parenti I., Kaiser F. J., Ehmke N. & Schaaf C. P. (20200206). Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies. : Genetics in medicine : official journal of the American College of Medical Genetics.
Chicago
Fountain Michael D, Oleson David S, Rech Megan E, Segebrecht Lara, Hunter Jill V, McCarthy John M, Lupo Philip J, Holtgrewe Manuel, Moran Rocio, Rosenfeld Jill A, Isidor Bertrand, Le Caignec Cédric, Saenz Margarita S, Pedersen Robert C, Morgan Thomas M, Pfotenhauer Jean P, Xia Fan, Bi Weimin, Kang Sung-Hae L, Patel Ankita, Krantz Ian D, Raible Sarah E, Smith Wendy, Cristian Ingrid, Torti Erin, Juusola Jane, Millan Francisca, Wentzensen Ingrid M, Person Richard E, Küry Sébastien, Bézieau Stéphane, Uguen Kévin, Férec Claude, Munnich Arnold, van Haelst Mieke, Lichtenbelt Klaske D, van Gassen Koen, Hagelstrom Tanner, Chawla Aditi, Perry Denise L, Taft Ryan J, Jones Marilyn, Masser-Frye Diane, Dyment David, Venkateswaran Sunita, Li Chumei, Escobar Luis F, Horn Denise, Spillmann Rebecca C, Peña Loren, Wierzba Jolanta, Strom Tim M, Parenti Ilaria, Kaiser Frank J, Ehmke Nadja and Schaaf Christian P. 20200206. Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies. : Genetics in medicine : official journal of the American College of Medical Genetics.
Harvard
Fountain M. D., Oleson D. S., Rech M. E., Segebrecht L., Hunter J. V., McCarthy J. M., Lupo P. J., Holtgrewe M., Moran R., Rosenfeld J. A., Isidor B., Le Caignec C., Saenz M. S., Pedersen R. C., Morgan T. M., Pfotenhauer J. P., Xia F., Bi W., Kang S. L., Patel A., Krantz I. D., Raible S. E., Smith W., Cristian I., Torti E., Juusola J., Millan F., Wentzensen I. M., Person R. E., Küry S., Bézieau S., Uguen K., Férec C., Munnich A., van Haelst M., Lichtenbelt K. D., van Gassen K., Hagelstrom T., Chawla A., Perry D. L., Taft R. J., Jones M., Masser-Frye D., Dyment D., Venkateswaran S., Li C., Escobar L. F., Horn D., Spillmann R. C., Peña L., Wierzba J., Strom T. M., Parenti I., Kaiser F. J., Ehmke N. and Schaaf C. P. (20200206). Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies. : Genetics in medicine : official journal of the American College of Medical Genetics.
MLA
Fountain Michael D, Oleson David S, Rech Megan E, Segebrecht Lara, Hunter Jill V, McCarthy John M, Lupo Philip J, Holtgrewe Manuel, Moran Rocio, Rosenfeld Jill A, Isidor Bertrand, Le Caignec Cédric, Saenz Margarita S, Pedersen Robert C, Morgan Thomas M, Pfotenhauer Jean P, Xia Fan, Bi Weimin, Kang Sung-Hae L, Patel Ankita, Krantz Ian D, Raible Sarah E, Smith Wendy, Cristian Ingrid, Torti Erin, Juusola Jane, Millan Francisca, Wentzensen Ingrid M, Person Richard E, Küry Sébastien, Bézieau Stéphane, Uguen Kévin, Férec Claude, Munnich Arnold, van Haelst Mieke, Lichtenbelt Klaske D, van Gassen Koen, Hagelstrom Tanner, Chawla Aditi, Perry Denise L, Taft Ryan J, Jones Marilyn, Masser-Frye Diane, Dyment David, Venkateswaran Sunita, Li Chumei, Escobar Luis F, Horn Denise, Spillmann Rebecca C, Peña Loren, Wierzba Jolanta, Strom Tim M, Parenti Ilaria, Kaiser Frank J, Ehmke Nadja and Schaaf Christian P. Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies. : Genetics in medicine : official journal of the American College of Medical Genetics. 20200206.