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	1.	Carrier screening by next-generation sequencing: health benefits and cost effectiveness. [electronic resource] by Azimi, Mohammad Schmaus, Kyle Greger, Valerie Neitzel, Dana Rochelle, Robert Dinh, Tuan Producer: 20160601 In: Molecular genetics & genomic medicine vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Truncating variants in the majority of the cytoplasmic domain of PCDH15 are unlikely to cause Usher syndrome 1F. [electronic resource] by Perreault-Micale, Cynthia Frieden, Alexander Kennedy, Caleb J Neitzel, Dana Sullivan, Jessica Faulkner, Nicole Hallam, Stephanie Greger, Valerie Producer: 20150608 In: The Journal of molecular diagnostics : JMD vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Validation for clinical use of, and initial clinical experience with, a novel approach to population-based carrier screening using high-throughput, next-generation DNA sequencing. [electronic resource] by Hallam, Stephanie Nelson, Heather Greger, Valerie Perreault-Micale, Cynthia Davie, Jocelyn Faulkner, Nicole Neitzel, Dana Casey, Kristie Umbarger, Mark A Chennagiri, Niru Kramer, Alexander C Porreca, Gregory J Kennedy, Caleb J Producer: 20141028 In: The Journal of molecular diagnostics : JMD vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)