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	1.	UPD detection using homozygosity profiling with a SNP genotyping microarray. [electronic resource] by Papenhausen, Peter Schwartz, Stuart Risheg, Hiba Keitges, Elisabeth Gadi, Inder Burnside, Rachel D Jaswaney, Vikram Pappas, John Pasion, Romela Friedman, Kenneth Tepperberg, James Producer: 20110830 In: American journal of medical genetics. Part A vol. 155A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotype. [electronic resource] by Burnside, Rachel D Pappas, John G Sacharow, Stephanie Applegate, Carolyn Hamosh, Ada Gadi, Inder K Jaswaney, Vikram Keitges, Elisabeth Phillips, Karen K Potluri, Venketaswara R Risheg, Hiba Smith, Janice L Tepperberg, Jim H Schwartz, Stuart Papenhausen, Peter Producer: 20130909 In: American journal of medical genetics. Part A vol. 161A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay. [electronic resource] by Burnside, Rachel D Pasion, Romela Mikhail, Fady M Carroll, Andrew J Robin, Nathaniel H Youngs, Erin L Gadi, Inder K Keitges, Elizabeth Jaswaney, Vikram L Papenhausen, Peter R Potluri, Venkateswara R Risheg, Hiba Rush, Brooke Smith, Janice L Schwartz, Stuart Tepperberg, James H Butler, Merlin G Producer: 20111114 In: Human genetics vol. 130 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)