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	1.	Segmental duplications mediate novel, clinically relevant chromosome rearrangements. [electronic resource] by Rudd, M Katharine Keene, Julia Bunke, Brian Kaminsky, Erin B Adam, Margaret P Mulle, Jennifer G Ledbetter, David H Martin, Christa L Producer: 20091027 In: Human molecular genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Towards a Universal Clinical Genomics Database: the 2012 International Standards for Cytogenomic Arrays Consortium Meeting. [electronic resource] by Riggs, Erin Rooney Wain, Karen E Riethmaier, Darlene Savage, Melissa Smith-Packard, Bethanny Kaminsky, Erin B Rehm, Heidi L Martin, Christa Lese Ledbetter, David H Faucett, W Andrew Producer: 20131230 In: Human mutation vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. [electronic resource] by Miller, David T Adam, Margaret P Aradhya, Swaroop Biesecker, Leslie G Brothman, Arthur R Carter, Nigel P Church, Deanna M Crolla, John A Eichler, Evan E Epstein, Charles J Faucett, W Andrew Feuk, Lars Friedman, Jan M Hamosh, Ada Jackson, Laird Kaminsky, Erin B Kok, Klaas Krantz, Ian D Kuhn, Robert M Lee, Charles Ostell, James M Rosenberg, Carla Scherer, Stephen W Spinner, Nancy B Stavropoulos, Dimitri J Tepperberg, James H Thorland, Erik C Vermeesch, Joris R Waggoner, Darrel J Watson, Michael S Martin, Christa Lese Ledbetter, David H Producer: 20100621 In: American journal of human genetics vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	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)
	5.	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)