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	1.	A pyrosequencing-based assay for the rapid detection of the 22q11.2 deletion in DNA from buccal and dried blood spot samples. [electronic resource] by Koontz, Deborah Baecher, Kirsten Kobrynski, Lisa Nikolova, Stanimila Gallagher, Margaret Producer: 20151016 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)
	2.	Rapid detection of the CYP2A6*12 hybrid allele by Pyrosequencing technology. [electronic resource] by Koontz, Deborah A Huckins, Jacqueline J Spencer, Antonina Gallagher, Margaret L Producer: 20090904 In: BMC medical genetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Influence of 5,10-methylenetetrahydrofolate reductase polymorphism on whole-blood folate concentrations measured by LC-MS/MS, microbiologic assay, and bio-rad radioassay. [electronic resource] by Fazili, Zia Pfeiffer, Christine M Zhang, Mindy Jain, Ram B Koontz, Deborah Producer: 20080212 In: Clinical chemistry vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	MALDI-TOF-MS Assay to Detect the Hemizygous 22q11.2 Deletion in DNA from Dried Blood Spots. [electronic resource] by Kobrynski, Lisa J Yazdanpanah, Golriz K Koontz, Deborah Lee, Francis K Vogt, Robert F Producer: 20160620 In: Clinical chemistry vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Folate-related gene variants in Irish families affected by neural tube defects. [electronic resource] by Fisk Green, Ridgely Byrne, Julianne Crider, Krista S Gallagher, Margaret Koontz, Deborah Berry, Robert J Producer: 20131113 In: Frontiers in genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Evaluation of mailed pediatric buccal cytobrushes for use in a case-control study of birth defects. [electronic resource] by Gallagher, Margaret L Sturchio, Cynthia Smith, Ashley Koontz, Deborah Jenkins, Mary M Honein, Margaret A Rasmussen, Sonja A Producer: 20111027 In: Birth defects research. Part A, Clinical and molecular teratology vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Prevalence and effects of gene-gene and gene-nutrient interactions on serum folate and serum total homocysteine concentrations in the United States: findings from the third National Health and Nutrition Examination Survey DNA Bank. [electronic resource] by Yang, Quan-He Botto, Lorenzo D Gallagher, Margaret Friedman, J M Sanders, Christopher L Koontz, Deborah Nikolova, Stanimila Erickson, J David Steinberg, Karen Producer: 20080731 In: The American journal of clinical nutrition vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Maternal smoking, xenobiotic metabolizing enzyme gene variants, and gastroschisis risk. [electronic resource] by Jenkins, Mary M Reefhuis, Jennita Gallagher, Margaret L Mulle, Jennifer G Hoffmann, Thomas J Koontz, Deborah A Sturchio, Cynthia Rasmussen, Sonja A Witte, John S Richter, Patricia Honein, Margaret A Producer: 20150113 In: American journal of medical genetics. Part A vol. 164A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Genetic studies of a cluster of acute lymphoblastic leukemia cases in Churchill County, Nevada. [electronic resource] by Steinberg, Karen K Relling, Mary V Gallagher, Margaret L Greene, Christopher N Rubin, Carol S French, Deborah Holmes, Adrianne K Carroll, William L Koontz, Deborah A Sampson, Eric J Satten, Glen A Producer: 20070502 In: Environmental health perspectives vol. 115 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Prothrombin G20210A mutation is associated with young-onset stroke: the genetics of early-onset stroke study and meta-analysis. [electronic resource] by Jiang, Baijia Ryan, Kathleen A Hamedani, Ali Cheng, Yuching Sparks, Mary J Koontz, Deborah Bean, Christopher J Gallagher, Margaret Hooper, W Craig McArdle, Patrick F O'Connell, Jeffrey R Stine, O Colin Wozniak, Marcella A Stern, Barney J Mitchell, Braxton D Kittner, Steven J Cole, John W Producer: 20140610 In: Stroke vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)