Additional file 6: of Identification of novel candidate disease genes from de novo exonic copy number variants

Gambin, Tomasz; Yuan, Bo; Bi, Weimin; Liu, Pengfei; Rosenfeld, Jill; Coban-Akdemir, Zeynep; Pursley, Amber; Nagamani, Sandesh; Marom, Ronit; Golla, Sailaja; Dengle, Lauren; Petrie, Heather; Matalon, Reuben; Emrick, Lisa; Proud, Monica; Treadwell-Deering, Diane; Chao, Hsiao-Tuan; Koillinen, Hannele; Brown, Chester; Urraca, Nora; Mostafavi, Roya; Bernes, Saunder; Roeder, Elizabeth; Nugent, Kimberly; Bader, Patricia; Bellus, Gary; Cummings, Michael; Northrup, Hope; Ashfaq, Myla; Westman, Rachel; Wildin, Robert; Beck, Anita; Immken, LaDonna; Elton, Lindsay; Varghese, Shaun; Buchanan, Edward; Faivre, Laurence; Lefebvre, Mathilde; Schaaf, Christian; Walkiewicz, Magdalena; Yang, Yaping; Kang, Sung-Hae; Lalani, Seema; Bacino, Carlos; Beaudet, Arthur; Breman, Amy; Smith, Janice; Cheung, Sau; Lupski, James; Patel, Ankita; Shaw, Chad; Stankiewicz, PaweĹ

doi:10.6084/m9.figshare.c.3886552_D6.v1

13073_2017_472_MOESM6_ESM.docx (21.88 kB)

Additional file 6: of Identification of novel candidate disease genes from de novo exonic copy number variants

journal contribution

posted on 2017-09-21, 05:00 authored by Tomasz Gambin, Bo Yuan, Weimin Bi, Pengfei Liu, Jill Rosenfeld, Zeynep Coban-Akdemir, Amber Pursley, Sandesh Nagamani, Ronit Marom, Sailaja Golla, Lauren Dengle, Heather Petrie, Reuben Matalon, Lisa Emrick, Monica Proud, Diane Treadwell-Deering, Hsiao-Tuan Chao, Hannele Koillinen, Chester Brown, Nora Urraca, Roya Mostafavi, Saunder Bernes, Elizabeth Roeder, Kimberly Nugent, Patricia Bader, Gary Bellus, Michael Cummings, Hope Northrup, Myla Ashfaq, Rachel Westman, Robert Wildin, Anita Beck, LaDonna Immken, Lindsay Elton, Shaun Varghese, Edward Buchanan, Laurence Faivre, Mathilde Lefebvre, Christian Schaaf, Magdalena Walkiewicz, Yaping Yang, Sung-Hae Kang, Seema Lalani, Carlos Bacino, Arthur Beaudet, Amy Breman, Janice Smith, Sau Cheung, James Lupski, Ankita Patel, Chad Shaw, PaweĹ Stankiewicz

Supplementary table containing clinical information on patients with CSMD1 variants. (DOCX 21 kb)

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National Institutes of Health (US)

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Exon targeted array CGH Intragenic copy number variants CNVs de novo variants

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Additional file 6: of Identification of novel candidate disease genes from de novo exonic copy number variants

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