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	1.	Single nucleotide polymorphisms in clinical genetic testing: the characterization of the clinical significance of genetic variants and their application in clinical research for BRCA1. [electronic resource] by Judkins, Thaddeus Hendrickson, Brant C Deffenbaugh, Amie M Scholl, Thomas Producer: 20050525 In: Mutation research vol. 573 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A GC-wave correction algorithm that improves the analytical performance of aCGH. [electronic resource] by Leo, Angela Walker, Andrew M Lebo, Matthew S Hendrickson, Brant Scholl, Thomas Akmaev, Viatcheslav R Producer: 20130228 In: The Journal of molecular diagnostics : JMD vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Two rare novel polymorphisms in the D8S1179 and D13S317 markers and method to mitigate their impact on human identification. [electronic resource] by Forrest, Shawn W Kupferschmid, Timothy D Hendrickson, Brant C Judkins, Thaddeus Petersen, Daniel J Scholl, Thomas Producer: 20041015 In: Croatian medical journal vol. 45 Availability: No items available. Save to lists Add to cart (remove)
	4.	A multi-exonic BRCA1 deletion identified in multiple families through single nucleotide polymorphism haplotype pair analysis and gene amplification with widely dispersed primer sets. [electronic resource] by Ward, Benjamin D Hendrickson, Brant C Judkins, Thaddeus Deffenbaugh, Amie M Leclair, Benoît Ward, Brian E Scholl, Thomas Producer: 20050621 In: The Journal of molecular diagnostics : JMD vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Accurate STR allele designations at the FGA and vWA loci despite primer site polymorphisms. [electronic resource] by Hendrickson, Brant C Leclair, Benoit Forrest, Shawn Ryan, John Ward, Brian E Petersen, Daniel Kupferschmid, Timothy D Scholl, Thomas Producer: 20040422 In: Journal of forensic sciences vol. 49 Availability: No items available. Save to lists Add to cart (remove)
	6.	Bioinformatics and human identification in mass fatality incidents: the world trade center disaster. [electronic resource] by Leclair, Benoît Shaler, Robert Carmody, George R Eliason, Kristilyn Hendrickson, Brant C Judkins, Thad Norton, Michael J Sears, Christopher Scholl, Tom Producer: 20070829 In: Journal of forensic sciences vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Application of embryonic lethal or other obvious phenotypes to characterize the clinical significance of genetic variants found in trans with known deleterious mutations. [electronic resource] by Judkins, Thaddeus Hendrickson, Brant C Deffenbaugh, Amie M Eliason, Kristilyn Leclair, Benoît Norton, Michael J Ward, Brian E Pruss, Dmitri Scholl, Thomas Producer: 20051222 In: Cancer research vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	A biochemical analysis demonstrates that the BRCA1 intronic variant IVS10-2A--> C is a mutation. [electronic resource] by Keaton, Jessica C Nielsen, David R Hendrickson, Brant C Pyne, Michael T Scheuer, Lauren Ward, Brian E Brothman, Arthur R Scholl, Thomas Producer: 20031104 In: Journal of human genetics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Prevalence of five previously reported and recurrent BRCA1 genetic rearrangement mutations in 20,000 patients from hereditary breast/ovarian cancer families. [electronic resource] by Hendrickson, Brant C Judkins, Thaddeus Ward, Benjamin D Eliason, Kristilyn Deffenbaugh, Amie E Burbidge, Lynn Anne Pyne, Kristin Leclair, Benoît Ward, Brian E Scholl, Thomas Producer: 20050726 In: Genes, chromosomes & cancer vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Evidence for common ancestral origin of a recurring BRCA1 genomic rearrangement identified in high-risk Hispanic families. [electronic resource] by Weitzel, Jeffrey N Lagos, Veronica I Herzog, Josef S Judkins, Thaddeus Hendrickson, Brant Ho, Jason S Ricker, Charité N Lowstuter, Katrina J Blazer, Kathleen R Tomlinson, Gail Scholl, Tom Producer: 20071011 In: Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72,400 specimens. [electronic resource] by Sugarman, Elaine A Nagan, Narasimhan Zhu, Hui Akmaev, Viatcheslav R Zhou, Zhaoqing Rohlfs, Elizabeth M Flynn, Kerry Hendrickson, Brant C Scholl, Thomas Sirko-Osadsa, Deborah Alexa Allitto, Bernice A Producer: 20120402 In: European journal of human genetics : EJHG vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Multiple rare nonsynonymous variants in the adenomatous polyposis coli gene predispose to colorectal adenomas. [electronic resource] by Azzopardi, Duncan Dallosso, Anthony R Eliason, Kristilyn Hendrickson, Brant C Jones, Natalie Rawstorne, Edward Colley, James Moskvina, Valentina Frye, Cynthia Sampson, Julian R Wenstrup, Richard Scholl, Thomas Cheadle, Jeremy P Producer: 20080214 In: Cancer research vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Prediction of MLH1 and MSH2 mutations in Lynch syndrome. [electronic resource] by Balmaña, Judith Stockwell, David H Steyerberg, Ewout W Stoffel, Elena M Deffenbaugh, Amie M Reid, Julia E Ward, Brian Scholl, Thomas Hendrickson, Brant Tazelaar, John Burbidge, Lynn Anne Syngal, Sapna Producer: 20060929 In: JAMA vol. 296 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Does the survival motor neuron copy number variation play a role in the onset and severity of sporadic amyotrophic lateral sclerosis in Malians? [electronic resource] by Sangare, Modibo Dicko, Ilo Guinto, Cheick Oumar Sissoko, Adama Dembele, Kekouta Coulibaly, Youlouza Coulibaly, Siaka Y Landoure, Guida Diallo, Abdallah Dolo, Mamadou Dolo, Housseini Maiga, Boubacar Traore, Moussa Karembe, Mamadou Traore, Kadiatou Toure, Amadou Sylla, Mariam Togora, Arouna Coulibaly, Souleymane Traore, Sékou Fantamady Hendrickson, Brant Bricceno, Katherine Schindler, Alice B Kokkinis, Angela Meilleur, Katherine G Sangho, Hammadoun Ali Diakite, Brehima Kassogue, Yaya Coulibaly, Yaya Ibrahim Burnett, Barrington Maiga, Youssoufa Doumbia, Seydou Fischbeck, Kenneth H Publication details: eNeurologicalSci Jun 2016 In: eNeurologicalSci vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Genetics of low spinal muscular atrophy carrier frequency in sub-Saharan Africa. [electronic resource] by Sangaré, Modibo Hendrickson, Brant Sango, Hammadoun Ali Chen, Kelian Nofziger, Jonathan Amara, Abdelbasset Dutra, Amalia Schindler, Alice B Guindo, Aldiouma Traoré, Mahamadou Harmison, George Pak, Evgenia Yaro, Fatoumata N'Go Bricceno, Katherine Grunseich, Christopher Chen, Guibin Boehm, Manfred Zukosky, Kristen Bocoum, Nouhoum Meilleur, Katherine G Daou, Fatoumata Bagayogo, Koumba Coulibaly, Yaya Ibrahim Diakité, Mahamadou Fay, Michael P Lee, Hee-Suk Saad, Ali Gribaa, Moez Singleton, Andrew B Maiga, Youssoufa Auh, Sungyoung Landouré, Guida Fairhurst, Rick M Burnett, Barrington G Scholl, Thomas Fischbeck, Kenneth H Producer: 20140617 In: Annals of neurology vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)