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	1.	Assessing the utility of confirmatory studies following identification of large-scale genomic imbalances by microarray. [electronic resource] by Sanmann, Jennifer N Pickering, Diane L Golden, Denae M Stevens, Jadd M Hempel, Thomas E Althof, Pamela A Wiggins, Michele L Starr, Lois J Davé, Bhavana J Sanger, Warren G Producer: 20160909 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar. [electronic resource] by Riggs, Erin R Nelson, Tristan Merz, Andrew Ackley, Todd Bunke, Brian Collins, Christin D Collinson, Morag N Fan, Yao-Shan Goodenberger, McKinsey L Golden, Denae M Haglund-Hazy, Linda Krgovic, Danijela Lamb, Allen N Lewis, Zoe Li, Guang Liu, Yajuan Meck, Jeanne Neufeld-Kaiser, Whitney Runke, Cassandra K Sanmann, Jennifer N Stavropoulos, Dimitri J Strong, Emma Su, Meng Tayeh, Marwan K Kokalj Vokac, Nadja Thorland, Erik C Andersen, Erica Martin, Christa L Producer: 20190820 In: Human mutation vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities. [electronic resource] by Kaminsky, Erin B Kaul, Vineith Paschall, Justin Church, Deanna M Bunke, Brian Kunig, Dawn Moreno-De-Luca, Daniel Moreno-De-Luca, Andres Mulle, Jennifer G Warren, Stephen T Richard, Gabriele Compton, John G Fuller, Amy E Gliem, Troy J Huang, Shuwen Collinson, Morag N Beal, Sarah J Ackley, Todd Pickering, Diane L Golden, Denae M Aston, Emily Whitby, Heidi Shetty, Shashirekha Rossi, Michael R Rudd, M Katharine South, Sarah T Brothman, Arthur R Sanger, Warren G Iyer, Ramaswamy K Crolla, John A Thorland, Erik C Aradhya, Swaroop Ledbetter, David H Martin, Christa L Producer: 20120327 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia. [electronic resource] by Moreno-De-Luca, Daniel Mulle, Jennifer G Kaminsky, Erin B Sanders, Stephan J Myers, Scott M Adam, Margaret P Pakula, Amy T Eisenhauer, Nancy J Uhas, Kim Weik, LuAnn Guy, Lisa Care, Melanie E Morel, Chantal F Boni, Charlotte Salbert, Bonnie Anne Chandrareddy, Ashadeep Demmer, Laurie A Chow, Eva W C Surti, Urvashi Aradhya, Swaroop Pickering, Diane L Golden, Denae M Sanger, Warren G Aston, Emily Brothman, Arthur R Gliem, Troy J Thorland, Erik C Ackley, Todd Iyer, Ram Huang, Shuwen Barber, John C Crolla, John A Warren, Stephen T Martin, Christa L Ledbetter, David H Producer: 20110124 In: American journal of human genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)