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	1.	Patients with mosaic methylation patterns of the Prader-Willi/Angelman Syndrome critical region exhibit AS-like phenotypes with some PWS features. [electronic resource] by Aypar, Umut Hoppman, Nicole L Thorland, Erik C Dawson, D Brian Producer: 20160323 In: Molecular cytogenetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Utility of microsatellite analysis in evaluation of pregnancies with placental mesenchymal dysplasia. [electronic resource] by Schuetzle, Marie N Uphoff, Timothy S Hatten, Bonnie A Dawson, D Brian Producer: 20080325 In: Prenatal diagnosis vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	C9orf72 Repeat Expansion Frequency among Patients with Huntington Disease Genetic Testing. [electronic resource] by Ida, Cristiane M Butz, Malinda L Lundquist, Patrick A Dawson, D Brian Producer: 20191002 In: Neuro-degenerative diseases vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Development and clinical implementation of a combination deletion PCR and multiplex ligation-dependent probe amplification assay for detecting deletions involving the human α-globin gene cluster. [electronic resource] by Kipp, Benjamin R Roellinger, Samantha E Lundquist, Patrick A Highsmith, W Edward Dawson, D Brian Producer: 20120105 In: The Journal of molecular diagnostics : JMD vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Development of real-time PCR assays for the quantitative detection of Epstein-Barr virus and cytomegalovirus, comparison of TaqMan probes, and molecular beacons. [electronic resource] by Jebbink, Jiska Bai, Xin Rogers, Beverly Barton Dawson, D Brian Scheuermann, Richard H Domiati-Saad, Rana Producer: 20030731 In: The Journal of molecular diagnostics : JMD vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Clinical diagnostic testing for the cytogenetic and molecular causes of male infertility: the Mayo Clinic experience. [electronic resource] by Hofherr, Sean E Wiktor, Anne E Kipp, Benjamin R Dawson, D Brian Van Dyke, Daniel L Producer: 20120316 In: Journal of assisted reproduction and genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Does parent of origin matter? Methylation studies should be performed on patients with multiple copies of the Prader-Willi/Angelman syndrome critical region. [electronic resource] by Aypar, Umut Brodersen, Pamela R Lundquist, Patrick A Dawson, D Brian Thorland, Erik C Hoppman, Nicole Producer: 20150604 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)
	8.	A Suggested Molecular Pathology Curriculum for Residents: A Report of the Association for Molecular Pathology. [electronic resource] by Aisner, Dara L Berry, Anna Dawson, D Brian Hayden, Randall T Joseph, Loren Hill, Charles E Producer: 20161031 In: The Journal of molecular diagnostics : JMD vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Partial hexasomy for the Prader-Willi-Angelman syndrome critical region due to a maternally inherited large supernumerary marker chromosome. [electronic resource] by Hoppman-Chaney, Nicole L Dawson, D Brian Nguyen, Lai Sengupta, Sunanda Reynolds, Kara McPherson, Elizabeth Velagaleti, Gopalrao Producer: 20101115 In: American journal of medical genetics. Part A vol. 152A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Primary effusion lymphomas exhibit complex and recurrent cytogenetic abnormalities. [electronic resource] by Wilson, Kathleen S McKenna, Robert W Kroft, Steven H Dawson, D Brian Ansari, Qasim Schneider, Nancy R Producer: 20020306 In: British journal of haematology vol. 116 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Making a Genetic Diagnosis in a Level IV Neonatal Intensive Care Unit Population: Who, When, How, and at What Cost? [electronic resource] by Swaggart, Kayleigh A Swarr, Daniel T Tolusso, Leandra K He, Hua Dawson, D Brian Suhrie, Kristen R Producer: 20200601 In: The Journal of pediatrics vol. 213 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Trisomy 20 mosaicism caused by a maternal meiosis II error is associated with normal intellect but multiple congenital anomalies. [electronic resource] by Ensenauer, Regina E Shaughnessy, William J Jalal, Syed M Dawson, D Brian Courteau, Laura K Ellison, Jay W Producer: 20050627 In: American journal of medical genetics. Part A vol. 134A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Central Diabetes Insipidus in a Patient With NFKB2 Mutation: Expanding the Endocrine Phenotype in DAVID Syndrome. [electronic resource] by Nasomyont, Nat Lindsley, Andrew W Assa'ad, Amal Dawson, D Brian Neilson, Derek E Brady, Cassandra C Rutter, Meilan M Publication details: The Journal of clinical endocrinology and metabolism Sep 2019 In: The Journal of clinical endocrinology and metabolism vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Hb Memphis [HBA2: c.70G>C (or HBA1)] in a Turkish child: a case report and comparison to Hb Q-Thailand (HBA1: c.223G>C). [electronic resource] by Lubrano, Lauren Donnelly, Michael J Sandler, Gerald Hoyer, James D Swanson, Kenneth C Dawson, D Brian Oliveira, Jennifer L Producer: 20141203 In: Hemoglobin vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Comprehensive mutation screening in 55 probands with type 1 primary hyperoxaluria shows feasibility of a gene-based diagnosis. [electronic resource] by Monico, Carla G Rossetti, Sandro Schwanz, Heidi A Olson, Julie B Lundquist, Patrick A Dawson, D Brian Harris, Peter C Milliner, Dawn S Producer: 20071206 In: Journal of the American Society of Nephrology : JASN vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Diagnosis of alpha-1-antitrypsin deficiency: An algorithm of quantification, genotyping, and phenotyping. [electronic resource] by Snyder, Melissa R Katzmann, Jerry A Butz, Malinda L Wiley, Carmen Yang, Ping Dawson, D Brian Halling, Kevin C Highsmith, W Edward Thibodeau, Stephen N Producer: 20070202 In: Clinical chemistry vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Four new beta chain hemoglobin variants without clinical or hematological effects: Hb San Bruno [beta39(C5)Gln-->His]; Hb Fort Dodge [beta93(F9)Cys-Tyr]; Hb Rhode Island [beta116(G18)His-->Tyr]; and Hb Inglewood [beta142(H20)Ala-->Thr]. [electronic resource] by Hoyer, James D McCormick, Daniel J Snow, Karen Kubik, Kathleen S Holmes, Michael W Dawson, D Brian Shaber, Ruth Marner, Mark Hosmer, Jennifer Shinno, Nancy Fairbanks, Virgil F Producer: 20030701 In: Hemoglobin vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Hb Grand Junction (HBB: c.348_349delinsG; p.His117IlefsX42): a new hyperunstable hemoglobin variant. [electronic resource] by Kent, Michael W Oliveira, Jennifer L Hoyer, James D Swanson, Kenneth C Kluge, Michelle L Dawson, D Brian Liang, Xiayuan Winkler, Tyler J Breaux, Charles W LaCount, Rachel Silliman, Christopher C Producer: 20140911 In: Hemoglobin vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Target-enrichment sequencing and copy number evaluation in inherited polyneuropathy. [electronic resource] by Wang, Wei Wang, Chen Dawson, D Brian Thorland, Erik C Lundquist, Patrick A Eckloff, Bruce W Wu, Yanhong Baheti, Saurabh Evans, Jared M Scherer, Steven S Dyck, Peter J Klein, Christopher J Producer: 20170428 In: Neurology vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Liver transplant-associated graft-versus-host disease. [electronic resource] by Smith, Douglas M Agura, Edward Netto, George Collins, Robert Levy, Marlon Goldstein, Robert Christensen, Laura Baker, Judy Altrabulsi, Basel Osowski, Lori McCormack, Jeff Fichtel, Lisa Dawson, D Brian Domiati-Saad, Rana Stone, Marvin Klintmalm, Goran Producer: 20030206 In: Transplantation vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 22 results.