APA
Gambin T., Yuan B., Bi W., Liu P., Rosenfeld J. A., Coban-Akdemir Z., Pursley A. N., Nagamani S. C. S., Marom R., Golla S., Dengle L., Petrie H. G., Matalon R., Emrick L., Proud M. B., Treadwell-Deering D., Chao H., Koillinen H., Brown C., Urraca N., Mostafavi R., Bernes S., Roeder E. R., Nugent K. M., Bader P. I., Bellus G., Cummings M., Northrup H., Ashfaq M., Westman R., Wildin R., Beck A. E., Immken L., Elton L., Varghese S., Buchanan E., Faivre L., Lefebvre M., Schaaf C. P., Walkiewicz M., Yang Y., Kang S. L., Lalani S. R., Bacino C. A., Beaudet A. L., Breman A. M., Smith J. L., Cheung S. W., Lupski J. R., Patel A., Shaw C. A. & Stankiewicz P. (20180618). Identification of novel candidate disease genes from de novo exonic copy number variants. : Genome medicine.
Chicago
Gambin Tomasz, Yuan Bo, Bi Weimin, Liu Pengfei, Rosenfeld Jill A, Coban-Akdemir Zeynep, Pursley Amber N, Nagamani Sandesh C S, Marom Ronit, Golla Sailaja, Dengle Lauren, Petrie Heather G, Matalon Reuben, Emrick Lisa, Proud Monica B, Treadwell-Deering Diane, Chao Hsiao-Tuan, Koillinen Hannele, Brown Chester, Urraca Nora, Mostafavi Roya, Bernes Saunder, Roeder Elizabeth R, Nugent Kimberly M, Bader Patricia I, Bellus Gary, Cummings Michael, Northrup Hope, Ashfaq Myla, Westman Rachel, Wildin Robert, Beck Anita E, Immken LaDonna, Elton Lindsay, Varghese Shaun, Buchanan Edward, Faivre Laurence, Lefebvre Mathilde, Schaaf Christian P, Walkiewicz Magdalena, Yang Yaping, Kang Sung-Hae L, Lalani Seema R, Bacino Carlos A, Beaudet Arthur L, Breman Amy M, Smith Janice L, Cheung Sau Wai, Lupski James R, Patel Ankita, Shaw Chad A and Stankiewicz Paweł. 20180618. Identification of novel candidate disease genes from de novo exonic copy number variants. : Genome medicine.
Harvard
Gambin T., Yuan B., Bi W., Liu P., Rosenfeld J. A., Coban-Akdemir Z., Pursley A. N., Nagamani S. C. S., Marom R., Golla S., Dengle L., Petrie H. G., Matalon R., Emrick L., Proud M. B., Treadwell-Deering D., Chao H., Koillinen H., Brown C., Urraca N., Mostafavi R., Bernes S., Roeder E. R., Nugent K. M., Bader P. I., Bellus G., Cummings M., Northrup H., Ashfaq M., Westman R., Wildin R., Beck A. E., Immken L., Elton L., Varghese S., Buchanan E., Faivre L., Lefebvre M., Schaaf C. P., Walkiewicz M., Yang Y., Kang S. L., Lalani S. R., Bacino C. A., Beaudet A. L., Breman A. M., Smith J. L., Cheung S. W., Lupski J. R., Patel A., Shaw C. A. and Stankiewicz P. (20180618). Identification of novel candidate disease genes from de novo exonic copy number variants. : Genome medicine.
MLA
Gambin Tomasz, Yuan Bo, Bi Weimin, Liu Pengfei, Rosenfeld Jill A, Coban-Akdemir Zeynep, Pursley Amber N, Nagamani Sandesh C S, Marom Ronit, Golla Sailaja, Dengle Lauren, Petrie Heather G, Matalon Reuben, Emrick Lisa, Proud Monica B, Treadwell-Deering Diane, Chao Hsiao-Tuan, Koillinen Hannele, Brown Chester, Urraca Nora, Mostafavi Roya, Bernes Saunder, Roeder Elizabeth R, Nugent Kimberly M, Bader Patricia I, Bellus Gary, Cummings Michael, Northrup Hope, Ashfaq Myla, Westman Rachel, Wildin Robert, Beck Anita E, Immken LaDonna, Elton Lindsay, Varghese Shaun, Buchanan Edward, Faivre Laurence, Lefebvre Mathilde, Schaaf Christian P, Walkiewicz Magdalena, Yang Yaping, Kang Sung-Hae L, Lalani Seema R, Bacino Carlos A, Beaudet Arthur L, Breman Amy M, Smith Janice L, Cheung Sau Wai, Lupski James R, Patel Ankita, Shaw Chad A and Stankiewicz Paweł. Identification of novel candidate disease genes from de novo exonic copy number variants. : Genome medicine. 20180618.