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	1.	Free the data: one laboratory's approach to knowledge-based genomic variant classification and preparation for EMR integration of genomic data. [electronic resource] by Bean, Lora J H Tinker, Stuart W da Silva, Cristina Hegde, Madhuri R Producer: 20140228 In: Human mutation vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Investigation of factors associated with paternal nondisjunction of chromosome 21. [electronic resource] by Oliver, Tiffany Renee Bhise, Archit Feingold, Eleanor Tinker, Stuart Masse, Nirupama Sherman, Stephanie L Producer: 20090930 In: American journal of medical genetics. Part A vol. 149A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	The FMR1 premutation and attention-deficit hyperactivity disorder (ADHD): evidence for a complex inheritance. [electronic resource] by Hunter, Jessica Ezzell Epstein, Michael P Tinker, Stuart W Abramowitz, Ann Sherman, Stephanie L Producer: 20120912 In: Behavior genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Fragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severity. [electronic resource] by Hunter, Jessica Ezzell Epstein, Michael P Tinker, Stuart W Charen, Krista H Sherman, Stephanie L Producer: 20081023 In: Genetic epidemiology vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	New insights into human nondisjunction of chromosome 21 in oocytes. [electronic resource] by Oliver, Tiffany Renee Feingold, Eleanor Yu, Kai Cheung, Vivian Tinker, Stuart Yadav-Shah, Maneesha Masse, Nirupama Sherman, Stephanie L Producer: 20080612 In: PLoS genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Linkage disequilibrium mapping in trisomic populations: analytical approaches and an application to congenital heart defects in Down syndrome. [electronic resource] by Kerstann, Kimberly F Feingold, Eleanor Freeman, Sallie B Bean, Lora J H Pyatt, Robert Tinker, Stuart Jewel, Amy H Capone, George Sherman, Stephanie L Producer: 20050217 In: Genetic epidemiology vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	An examination of the relationship between hotspots and recombination associated with chromosome 21 nondisjunction. [electronic resource] by Oliver, Tiffany Renee Middlebrooks, Candace D Tinker, Stuart W Allen, Emily Graves Bean, Lora J H Begum, Ferdouse Feingold, Eleanor Chowdhury, Reshmi Cheung, Vivian Sherman, Stephanie L Producer: 20151026 In: PloS one vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21. [electronic resource] by Middlebrooks, Candace D Mukhopadhyay, Nandita Tinker, Stuart W Allen, Emily Graves Bean, Lora J H Begum, Ferdouse Chowdhury, Reshmi Cheung, Vivian Doheny, Kimberly Adams, Marcia Feingold, Eleanor Sherman, Stephanie L Producer: 20140805 In: Human molecular genetics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21. [electronic resource] by Oliver, Tiffany Renee Tinker, Stuart W Allen, Emily Graves Hollis, Natasha Locke, Adam E Bean, Lora J H Chowdhury, Reshmi Begum, Ferdouse Marazita, Mary Cheung, Vivian Feingold, Eleanor Sherman, Stephanie L Producer: 20120824 In: Human genetics vol. 131 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	The National Down Syndrome Project: design and implementation. [electronic resource] by Freeman, Sallie B Allen, Emily G Oxford-Wright, Cindy L Tinker, Stuart W Druschel, Charlotte Hobbs, Charlotte A O'Leary, Leslie A Romitti, Paul A Royle, Marjorie H Torfs, Claudine P Sherman, Stephanie L Producer: 20070206 In: Public health reports (Washington, D.C. : 1974) vol. 122 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome Project. [electronic resource] by Freeman, Sallie B Bean, Lora H Allen, Emily G Tinker, Stuart W Locke, Adam E Druschel, Charlotte Hobbs, Charlotte A Romitti, Paul A Royle, Marjorie H Torfs, Claudine P Dooley, Kenneth J Sherman, Stephanie L Producer: 20080808 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: a report from the National Down Syndrome Project. [electronic resource] by Hollis, NaTasha D Allen, Emily G Oliver, Tiffany Renee Tinker, Stuart W Druschel, Charlotte Hobbs, Charlotte A O'Leary, Leslie A Romitti, Paul A Royle, Marjorie H Torfs, Claudine P Freeman, Sallie B Sherman, Stephanie L Bean, Lora J H Producer: 20130805 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)
	13.	Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: a report from the National Down Syndrome Project. [electronic resource] by Bean, Lora J H Allen, Emily G Tinker, Stuart W Hollis, Natasha D Locke, Adam E Druschel, Charlotte Hobbs, Charlotte A O'Leary, Leslie Romitti, Paul A Royle, Marjorie H Torfs, Claudine P Dooley, Kenneth J Freeman, Sallie B Sherman, Stephanie L Producer: 20111222 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)
	14.	Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome. [electronic resource] by Locke, Adam E Dooley, Kenneth J Tinker, Stuart W Cheong, Soo Yeon Feingold, Eleanor Allen, Emily G Freeman, Sallie B Torfs, Claudine P Cua, Clifford L Epstein, Michael P Wu, Michael C Lin, Xihong Capone, George Sherman, Stephanie L Bean, Lora J H Producer: 20110114 In: Genetic epidemiology vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)