Publications

  1. Pratt VM, Turner A, Broeckel U, Dawson DB, Gaedigk A, Lynnes TC, Medeiros EB, Moyer AM, Requesens D, Vetrini F, Kalman LV. Characterization of Reference Materials with an Association for Molecular Pathology Pharmacogenetics Working Group Tier 2 Status: CYP2C9, CYP2C19, VKORC1, CYP2C Cluster Variant, and GGCX: A GeT-RM Collaborative Project. J Mol Diagn. 2021 Aug; 23 (8):952-958 Epub 2021 May 19
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  2. Ida CM, Butz ML, Lundquist PA, Dawson DB. C9orf72 Repeat Expansion Frequency among Patients with Huntington Disease Genetic Testing. Neurodegener Dis. 2018; 18 (5-6):239-253 Epub 2018 Oct 18
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  3. Gao F, Festic E, Schultz M, Schultz M, Roberts JA, Dawson D, Garcia M, Jones A, Scott M. ESICM LIVES 2016: part one : Milan, Italy. 1-5 October 2016. Intensive Care Med Exp. 2016 Sep; 4: (Suppl 1)27.
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  4. Wang W, Wang C, Dawson DB, Thorland EC, Lundquist PA, Eckloff BW, Wu Y, Baheti S, Evans JM, Scherer SS, Dyck PJ, Klein CJ. Target-enrichment sequencing and copy number evaluation in inherited polyneuropathy. Neurology. 2016 May 10; 86 (19):1762-71 Epub 2016 Apr 13
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  5. Bateman RM, Sharpe MD, Jagger JE, Ellis CG, Sole-Violan J, Lopez-Rodriguez M, Herrera-Ramos E, Ruiz-Hernandez J, Borderias L, Horcajada J, Gonzalez-Quevedo N, Rajas O, Briones M, Rodriguez de Castro F, Rodriguez Gallego C, Esen F, Orhun G, Ergin Ozcan P, Senturk E, Ugur Yilmaz C, Orhan N, Arican N, Kaya M, Kucukerden M, Giris M, Akcan U, Bilgic Gazioglu S, Tuzun E, Riff R, Naamani O, Douvdevani A, Takegawa R, Yoshida H, Hirose T, Yamamoto N, Hagiya H, Ojima M, Akeda Y, Tasaki O, Tomono K, Shimazu T, Ono S, Kubo T, Suda S, Ueno T, Ikeda T, Hirose T, Ogura H, Takahashi H, Ojima M, Kang J, Nakamura Y, Kojima T, Shimazu T, Ikeda T, Suda S, Izutani Y, Ueno T, Ono S, Taniguchi T, O M, Dinter C, Lotz J, Eilers B, Wissmann C, Lott R, Meili MM, Schuetz PS, Hawa H, Sharshir M, Aburageila M, Salahuddin N, Chantziara V, Georgiou S, Tsimogianni A, Alexandropoulos P, Vassi A, Lagiou F, Valta M, Micha G, Chinou E, Michaloudis G, Kodaira A, Ikeda T, Ono S, Ueno T, Suda S, Izutani Y, Imaizumi H, De la Torre-Prados MV, Garcia-De la Torre A, Enguix-Armada A, Puerto-Morlan A, Perez-Valero V, Garcia-Alcantara A, Bolton N, Dudziak J, Bonney S, Tridente A, Nee P, Nicolaes G, Wiewel M, Schultz M, Wildhagen K, Horn J, Schrijver R, Van der Poll T, Reutelingsperger C, Pillai S, Davies G, Mills G, Aubrey R, Morris K, Williams P, Evans P, Gayat EG, Struck J, Cariou A, Deye N, Guidet B, Jabert S, Launay J, Legrand M, Leone M, Resche-Rigon M, Vicaut E, Vieillard-Baron A, Mebazaa A, Arnold R, Capan M, Linder A, Akesson P, Popescu M, Tomescu D, Sprung CL, Calderon Morales R, Munteanu G, Orenbuch-Harroch E, Levin P, Kasdan H, Reiter A, Volker T, Himmel Y, Cohen Y, Meissonnier J, Girard L, Rebeaud F, Herrmann I, Delwarde B, Peronnet E, Cerrato E, Venet F, Lepape A, Rimmele T, Monneret G, Textoris J, Beloborodova N, Moroz V, Osipov A, Bedova A, Sarshor Y, Pautova A, Sergeev A, Chernevskaya E, Odermatt J, Bolliger R, Hersberger L, Ottiger M, Christ-Crain M, Mueller B, Schuetz P, Sharma NK, Tashima AK, Brunialti MK, Machado FR, Assuncao M, Rigato O, Salomao R, Cajander SC, Rasmussen G, Tina E, Soderquist B, Kallman J, Stralin K, Lange AL, Sunden-Cullberg JS, Magnuson AM, Hultgren OH, Davies G, Pillai S, Mills G, Aubrey R, Morris K, Williams P, Evans P, Pillai S, Davies G, Mills G, Aubrey R, Morris K, Williams P, Evans P, Pillai S, Davies G, Mills G, Aubrey R, Morris K, Williams P, Burke JP, Dogan M, et al, S South Yorkshire Hospitals Research Collaboration, Singer J, Boyd J, Roy S, Lambert ML, Dang T, Fernandez L, Jenkins SA, Griffin R, Lujan J, Dawson D, Zhang P, Basu A, Hussain I, Desai N, Lin S, Radosevich M, Wanta B, Diedrich D, Adams A, O'Neill L, Hurst T, Park C, Dickinson MG, Ramirez S, Horibe M, Evers S, Anwar S, White JC, Peters M, Butler M, Valdez C, Lee SD, Peters C, McPhail M, Song S, Marshall R, Lynch C, Stott D, Varma A, Miranda L, Neill A, Galvez R, Fernandez A, Walsh C. 36th International Symposium on Intensive Care and Emergency Medicine : Brussels, Belgium. 15-18 March 2016. Crit Care. 2016 Apr 20; 20 (Suppl 2):94
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  6. Aisner DL, Berry A, Dawson DB, Hayden RT, Joseph L, Hill CE. A Suggested Molecular Pathology Curriculum for Residents: A Report of the Association for Molecular Pathology. J Mol Diagn. 2016 Mar; 18 (2):153-62 Epub 2016 Feb 05
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  7. Aypar U, Hoppman NL, Thorland EC, Dawson DB. Patients with mosaic methylation patterns of the Prader-Willi/Angelman Syndrome critical region exhibit AS-like phenotypes with some PWS features. Mol Cytogenet. 2016; 9:26 Epub 2016 Mar 22
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  8. Author et al al, Bateman RM, Sharpe MD, Jagger JE, Ellis CG, Sole-Violan J, Lopez-Rodriguez M, Herrera-Ramos E, Ruiz-Hernandez J, Borderias L, Horcajada J, Gonzalez-Quevedo N, Rajas O, Briones M, Rodriguez de Castro F, Rodriguez Gallego C, Esen F, Orhun G, Ergin Ozcan P, Senturk E, Ugur Yilmaz C, Orhan N, Arican N, Kaya M, Kucukerden M, Giris M, Akcan U, Bilgic Gazioglu S, Tuzun E, Riff R, Naamani O, Douvdevani A, Takegawa R, Yoshida H, Hirose T, Yamamoto N, Hagiya H, Ojima M, Akeda Y, Tasaki O, Tomono K, Shimazu T, Ono S, Kubo T, Suda S, Ueno T, Ikeda T, Hirose T, Ogura H, Takahashi H, Ojima M, Kang J, Nakamura Y, Kojima T, Shimazu T, Ikeda T, Suda S, Izutani Y, Ueno T, Ono S, Taniguchi T, O M, Dinter C, Lotz J, Eilers B, Wissmann C, Lott R, Meili MM, Schuetz PS, Hawa H, Sharshir M, Aburageila M, Salahuddin N, Chantziara V, Georgiou S, Tsimogianni A, Alexandropoulos P, Vassi A, Lagiou F, Valta M, Micha G, Chinou E, Michaloudis G, Kodaira A, Ikeda T, Ono S, Ueno T, Suda S, Izutani Y, Imaizumi H, De la Torre-Prados MV, Garcia-De la Torre A, Enguix-Armada A, Puerto-Morlan A, Perez-Valero V, Garcia-Alcantara A, Bolton N, Dudziak J, Bonney S, Tridente A, Nee P, Nicolaes G, Wiewel M, Schultz M, Wildhagen K, Horn J, Schrijver R, Van der Poll T, Reutelingsperger C, Pillai S, Davies G, Mills G, Aubrey R, Morris K, Williams P, Evans P, Gayat EG, Struck J, Cariou A, Deye N, Guidet B, Jabert S, Launay J, Legrand M, Leone M, Resche-Rigon M, Vicaut E, Vieillard-Baron A, Mebazaa A, Arnold R, Capan M, Linder A, Akesson P, Popescu M, Tomescu D, Sprung CL, Calderon Morales R, Munteanu G, Orenbuch-Harroch E, Levin P, Kasdan H, Reiter A, Volker T, Himmel Y, Cohen Y, Meissonnier J, Girard L, Rebeaud F, Herrmann I, Delwarde B, Peronnet E, Cerrato E, Venet F, Lepape A, Rimmele T, Monneret G, Textoris J, Beloborodova N, Moroz V, Osipov A, Bedova A, Sarshor Y, Pautova A, Sergeev A, Chernevskaya E, Odermatt J, Bolliger R, Hersberger L, Ottiger M, Christ-Crain M, Mueller B, Schuetz P, Sharma NK, Tashima AK, Brunialti MK, Machado FR, Assuncao M, Rigato O, Salomao R, Cajander SC, Rasmussen G, Tina E, Soderquist B, Kallman J, Stralin K, Lange AL, Sunden-Cullberg JS, Magnuson AM, Hultgren OH, Davies G, Pillai S, Mills G, Aubrey R, Morris K, Williams P, Evans P, Pillai S, Davies G, Mills G, Aubrey R, Morris K, Williams P, Evans P, Pillai S, Davies G, Mills G, Aubrey R, Morris K, Williams P, Evans P, Van der Geest P, Mohseni M, Linssen J, De Jonge R, Duran S, Groeneveld J, Miller III, Burke JP, Dogan M, et al, Singer J, Boyd J, Roy S, Carr B, Jones B, Lopez J, Dang T, Fernandez L, Rousseau A, Jenkins SA, Griffin R, Dawson D, Zhang P, Basu A, Hussain I, Desai N, Lin S, Park M, Lee C, Radosevich M, Wanta B, Diedrich D, Adams A, Hurst T, Park C, Dickinson MG, Vu LH, Ramirez S, Horibe M, Evers S, Dubois J, Anwar S, Peters M, Butler M, Valdez C, Pritchett C, Lee SD, Song S, Lynch C, Varma A, Carlson E, Miranda L, Neill A. Erratum to: 36th International Symposium on Intensive Care and Emergency Medicine: Brussels, Belgium. 15-18 March 2016. Crit Care. 2016; 20:347 Epub 2016 Oct 24
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  9. Aypar U, Brodersen PR, Lundquist PA, Dawson DB, Thorland EC, Hoppman N. Does parent of origin matter? Methylation studies should be performed on patients with multiple copies of the Prader-Willi/Angelman syndrome critical region. Am J Med Genet A. 2014 Oct; 164A (10):2514-20 Epub 2014 June 26
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  10. Kent MW, Oliveira JL, Hoyer JD, Swanson KC, Kluge ML, Dawson DB, Liang X, Winkler TJ, Breaux CW Jr, LaCount R, Silliman CC. Hb Grand Junction (HBB: c.348_349delinsG; p.His117IlefsX42): a new hyperunstable hemoglobin variant. Hemoglobin. 2014; 38(1):8-12.
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  11. Lubrano L, Donnelly MJ, Sandler G, Hoyer JD, Swanson KC, Dawson DB, Oliveira JL. 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). Hemoglobin. 2014; 38(2):137-41.
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  12. Hofherr SE, Wiktor AE, Kipp BR, Dawson DB, Van Dyke DL. Clinical diagnostic testing for the cytogenetic and molecular causes of male infertility: the Mayo Clinic experience. J Assist Reprod Genet. 2011 Nov; 28 (11):1091-8 Epub 2011 Sept 13
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  13. Kipp BR, Roellinger SE, Lundquist PA, Highsmith WE, Dawson DB. Development and clinical implementation of a combination deletion PCR and multiplex ligation-dependent probe amplification assay for detecting deletions involving the human alpha-globin gene cluster. J Mol Diagn. 2011 Sep; 13 (5):549-57 Epub 2011 June 25
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  14. Hoppman-Chaney NL, Dawson DB, Nguyen L, Sengupta S, Reynolds K, McPherson E, Velagaleti G. Partial hexasomy for the Prader-Willi-Angelman syndrome critical region due to a maternally inherited large supernumerary marker chromosome. Am J Med Genet A. 2010 Aug; 152A (8):2034-8
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  15. Schuetzle MN, Uphoff TS, Hatten BA, Dawson DB. Utility of microsatellite analysis in evaluation of pregnancies with placental mesenchymal dysplasia. Prenat Diagn. 2007 Dec; 27: (13)1238-44.
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  16. Monico CG, Rossetti S, Schwanz HA, Olson JB, Lundquist PA, Dawson DB, Harris PC, Milliner DS. Comprehensive mutation screening in 55 probands with type 1 primary hyperoxaluria shows feasibility of a gene-based diagnosis. J Am Soc Nephrol. 2007 Jun; 18(6):1905-14. Epub 2007 Apr 25.
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  17. Snyder MR, Katzmann JA, Butz ML, Wiley C, Yang P, Dawson DB, Halling KC, Highsmith WE, Highsmith WE, Thibodeau SN. Diagnosis of alpha-1-antitrypsin deficiency: An algorithm of quantification, genotyping, and phenotyping. Clin Chem. 2006 Dec; 52 (12):2236-42 Epub 2006 Oct 19
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  18. Ensenauer RE, Shaughnessy WJ, Jalal SM, Dawson DB, Courteau LK, Ellison JW. Trisomy 20 mosaicism caused by a maternal meiosis II error is associated with normal intellect but multiple congenital anomalies. Am J Med Genet Part A. 2005 Apr 15; 134A(2):202-6.
  19. Ensenauer RE, Shaughnessy WJ, Jalal SM, Dawson DB, Courteau LK, Ellison JW. Trisomy 20 mosaicism caused by a maternal meiosis II error is associated with normal intellect but multiple congenital anomalies. Am J Med Genet A. 2005 Apr 15; 134A (2):202-6
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  20. Ensenauer RE, Adeyinka A, Flynn HC, Michels VV, Lindor NM, Dawson DB, Thorland EC, Lorentz CP, Goldstein JL, McDonald MT, Smith WE, Simon-Fayard E, Alexander AA, Kulharya AS, Ketterling RP, Clark RD, Jalal SM. Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients. Am J Hum Genet. 2003 Nov; 73 (5):1027-40 Epub 2003 Oct 02
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  21. Jebbink J, Bai X, Rogers BB, Dawson DB, Scheuermann RH, Domiati-Saad R. Development of real-time PCR assays for the quantitative detection of Epstein-Barr virus and cytomegalovirus, comparison of TaqMan probes, and molecular beacons. J Mol Diagn. 2003 Feb; 5(1):15-20.
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  22. Smith DM, Agura E, Netto G, Collins R, Levy M, Goldstein R, Christensen L, Baker J, Altrabulsi B, Osowski L, McCormack J, Fichtel L, Dawson DB, Domiati-Saad R, Stone M, Klintmalm G. Liver transplant-associated graft-versus-host disease. Transplantation. 2003 Jan 15; 75(1):118-26.
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  23. Gonzalez-Yebra B, Salcedo M, Medrano ME, Mantilla A, Quinonez G, Benitez-Bribiesca L, Rodriguez-Cuevas S, Cabrera L, de Leon B, Altamirano N, Tapia J, Dawson DB. RET oncogene mutations in medullary thyroid carcinoma in Mexican families. Arch Med Res. 2003 Jan-Feb; 34(1):41-9.
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  24. Hoyer JD, McCormick DJ, Snow K, Kubik KS, Holmes MW, Dawson DB, Shaber R, Marner M, Hosmer J, Shinno N, Fairbanks VF. 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]. Hemoglobin. 2002 Aug; 26 (3):299-303
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  25. Wilson KS, McKenna RW, Kroft SH, Dawson DB, Ansari Q, Schneider NR. Primary effusion lymphomas exhibit complex and recurrent cytogenetic abnormalities. British J Haematology. 2002; 116:113-21.
  26. Breuer-McHam J, Simpson E, Dougherty I, Bonkobara M, Ariizumi K, Lewis DE, Dawson DB, Duvic M, Cruz PD. Activation of HIV in human skin by ultraviolet B radiation and its inhibition by NFkappaB blocking agents. Photochem Photobiol. 2001 Dec; 74(6):805-10.
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  27. Jamal S, Picker LJ, Aquino DB, McKenna RW, Dawson DB, Kroft SH. Immunophenotypic analysis of peripheral T-cell neoplasms. A multiparameter flow cytometric approach. Am J Clin Pathol. 2001 Oct; 116(4):512-26.
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  28. Kroft SH, Dawson DB, McKenna RW. Large cell lymphoma transformation of chronic lymphocytic leukemia/small lymphocytic lymphoma. A flow cytometric analysis of seven cases. Am J Clin Pathol. 2001 Mar; 115(3):385-95.
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  29. Bai X, Rogers BB, Harkins PC, Sommerauer J, Squires R, Rotondo K, Quan A, Dawson DB, Scheuermann RH. Predictive value of quantitative PCR-based viral burden analysis for eight human herpesviruses in pediatric solid organ transplant patients. J Molecular Diagnostics. 2001; 2:191-01.
  30. Roush KS, Domiati-Saad RK, Margraf LR, Krisher K, Scheuermann RH, Rogers BB, Dawson DB. Prevalence and cellular reservoir of latent human herpesvirus 6 in tonsillar lymphoid tissue. American Journal of Clinical Pathology 116(5) 2001.
  31. Kroft SH, Domiati-Saad R, Finn WG, Schnitzer B, Dawson DB, Singleton TP, Ross CW. Precursor B-Lymphoblastic transformation of grade I follicle center lymphoma. American Journal of Clinical Pathology. 2000 Mar; 113(3):411-18.
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  32. Domiati-Saad R, Dawson DB, Margraf LR, Finegold MJ, Weinberg AG, Rogers BB. Cytomegalovirus and human herpesvirus 6, but not human papillomavirus, are present in neonatal giant cell hepatitis and extrahepatic biliary atresia. Pediatric and Developmental Pathology. 2000; 3:367-73.
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  33. Hoang MP, Ross KF, Dawson DB, Scheuermann RH, Rogers BB. Human herpesvirus-6 and sudden death in infancy: Report of a case and review of the literature. Journal of Forensic Sciences. 1999 Mar; 44(2):432-37.
  34. Hoang MP, Rogers BB, Dawson DB, Scheuermann RH. Quantitation of the eight human herpesviruses in peripheral blood of human immunodeficiency virus positive individuals and healthy blood donors by polymerase chain reaction. Microbiology and Infectious Disease. 1999; 111:655-59.
  35. Dawson DB. The unique challenges and rewards of testing newborn infants. Clinical Chemistry News. 1998 Jul 24.
  36. Rogers BB, Sommerauer J, Quan A, Timmons CF, Dawson DB, Scheuermann RG, Krisher K, Atkins D. Epstein-Barr virus polymerase chain reaction and serology in pediatric post-transplant lymphoproliferative disorder: Three-year experience. Pediatric and Developmental Pathology. 1998; 1:480-86.
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  37. Hoang MP, Dawson DB, Rogers ZR, Scheuermann RH, Rogers BB. Polymerase chain reaction amplification of archival material for Epstein-Barr virus, cytomegalovirus, human herpesvirus 6, and parvovirus B19 in children with bone marrow hemophagocytosis. Human Pathology. 1998; 29:1074-77.
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  38. Siegelman M, Mohabeer A, Fahey TJ 3rd, Tomlinson G, Mayambala C, Jafari S, Noll WW, Thibodeau SN, Dawson DB. Rapid, nonradioactive screening for mutations in exons 10, 11, and 16 of the RET protooncogene associated with inherited medullary thyroid carcinoma. Clin Chem. 1997 Mar; 43(3):453-7.
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  39. Rogers BB, Conlin C, Timmons CF, Dawson DB, Krisher K, Andrews W. Epstein-Barr virus PCR correlated with viral histology and serology in pediatric liver transplant patients. Pediatric Pathology and Laboratory Medicine. 1997; 17:391-400.
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  40. Moghrabi NN, Naylor SL, Van Veldhoven PP, Baumgart E, Dawson DB, Bennett MJ. Assignment of the human peroxisomal branched-chain acyl-CoA oxidase gene to chromosome 3p21. 1-p14.2 by rodent/human somatic cell hybridization. Biochemical and Biophysical Research Communications. 1997; 231:767-69.
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  41. Bai X, Hosler G, Rogers BB, Dawson DB, Scheuermann RH. Quantitative PCR for human herpes virus diagnosis and measurement of Epstein-Barr virus burden in post-transplant lymphoproliferative disorder. Clinical Chemistry. 1997; 43:1843-49.
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  42. Kemp PM, Little BB, Bost RO, Dawson DB. Whole blood dodecanoic acid levels, a routinely detectable forensic marker for a genetic disease often misdiagnosed as sudden infant death syndrome (SIDS): MCAD deficiency. The American Journal of Forensic Medicine and Pathology. 1996; 17:79-82.
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  43. Ansari MQ, Dawson DB, Nador R, Rutherford C, Schneider NR, Latimer MJ, Picker L, Knowles DM, McKenna RW. Primary body cavity-based AIDS-related lymphomas. American Journal of Clinical Pathology. 1996; 105:221-9.
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  44. Nador RG, Cesarman E, Chadburn A, Dawson DB, Ansari MQ, Said J, Knowles DM. Primary effusion lymphoma: A distinct clinicopathologic entity associated with the Kaposi's sarcoma-associated herpesvirus. Blood. 1996; 88:645-56.
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  45. Zweiner RJ, Fielman BA, Cochran C, Rogers BB, Dawson DB, Timmons CF, Buchanan GR. Interferon alfa-2b treatment of chronic hepatitis C in children with hemophilia. Pediatric Infectious Disease Journal. 1996; 15:906-08.
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  46. Dawson DB, Jialal I. Multiple endocrine neoplasia. Diagnostic Endocrinology and Metabolism. 1996; 14:281-92.
  47. Dawson DB, Waber L, Hale D, Bennett M. Transient organic aciduria and persistent lactic acidemia in a patient with short-chain acyl-CoA dehydrogenase deficiency. The Journal of Pediatrics. 1995; 126:69-71.
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  48. Timmons CF, Dawson DB, Richard S, Andrews WS, Katz JA. Epstein-Barr virus-associated leiomyosarcomas in liver transplantation recipients: Origin from either donor or recipient tissue. Cancer. 1995; 76:1481-89.
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  49. Moghrabi NN, Dawson DB, Bennett MJ. Assignment of the human peroxisomal acyl-CoA oxidase gene to chromosome 17q23-qter by PCR technique. Journal of Inherited Metabolic Disease. 1995; 18:705-9.
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  50. Dawson DB. Erythrohepatic protoporphyria, liver transplantation and Guillain-Barré syndrome. Clinical Chemistry News. 1992 Apr.
  51. Dawson DB. Use of nucleic acid probes in genetic tests. Clinical Biochemistry. 1990; 23:279-85.
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  52. Dawson DB, Cummins LA, Schaid DJ, Michels VV, Gordon H, O'Connell EJ, Thibodeau SN. Carrier identification of cystic fibrosis by recombinant DNA techniques. Mayo Clin Proc. 1989 Mar; 64 (3):325-34
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  53. Dawson DB. DNA diagnostic use grows. Clinical Chemistry News. 1989 Sep 12.
  54. Dawson DB, Varandani PT. Characterization and application of monoclonal antibodies directed to separate epitopes of glutathione-insulin transhydrogenase. Biochimica et Biophisica Acta. 1987; 923:389-400.
  55. Dawson DB, Smith RA, Varandani PT. Production of a monoclonal antibody directed against rat liver glutathione-insulin transhydrogenase. Biochemical and Biophysical Research Communications. 1984; 125(2):668-74.
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