D. Dawson

R. Scheuermann, C. Timmons, D. Dawson, 1998, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Epstein-Barr virus PCR correlated with viral histology and serology in pediatric liver transplant patients.

C. Timmons, D. Dawson, B. Rogers, 1997, Pediatric pathology & laboratory medicine : journal of the Society for Pediatric Pathology, affiliated with the International Paediatric Pathology Association.

Whole blood levels of dodecanoic acid, a routinely detectable forensic marker for a genetic disease often misdiagnosed as sudden infant death syndrome (SIDS): MCAD deficiency.

D. Dawson, P. Kemp, B. Little, 1996, The American journal of forensic medicine and pathology.

Primary effusion lymphoma: a distinct clinicopathologic entity associated with the Kaposi's sarcoma-associated herpes virus.

E. Cesarman, D. Dawson, M. Ansari, 1996, Blood.

Development of real-time PCR assays for the quantitative detection of Epstein-Barr virus and cytomegalovirus, comparison of TaqMan probes, and molecular beacons.

R. Scheuermann, D. Dawson, B. Rogers, 2003, The Journal of molecular diagnostics : JMD.

Clinical diagnostic testing for the cytogenetic and molecular causes of male infertility: the Mayo Clinic experience

D. Dawson, S. Hofherr, B. Kipp, 2011, Journal of Assisted Reproduction and Genetics.

Cytomegalovirus and Human Herpesvirus 6, but Not Human Papillomavirus, Are Present in Neonatal Giant Cell Hepatitis and Extrahepatic Biliary Atresia

D. Dawson, L. Margraf, A. Weinberg, 2000, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Use of nucleic acid probes in genetic tests.

D. Dawson, 1990, Clinical biochemistry.

Partial hexasomy for the Prader–Willi–Angelman syndrome critical region due to a maternally inherited large supernumerary marker chromosome

D. Dawson, E. McPherson, G. Velagaleti, 2010, American journal of medical genetics. Part A.

Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients.

E. Thorland, N. Lindor, D. Dawson, 2003, American journal of human genetics.

Genetic Basis of Neurologic and Neuromuscular Diseases

S. Thibodeau, D. Dawson, C. Klein, 2006 .

Genetic Testing in Patients with Neurodevelopmental Disorders: Experience of 511 Patients at Cincinnati Children's Hospital Medical Center

D. Dawson, J. Glass, Xiaoli Du, 2021, Journal of Autism and Developmental Disorders.

Utility of microsatellite analysis in evaluation of pregnancies with placental mesenchymal dysplasia

D. Dawson, T. Uphoff, M. Schuetzle, 2007, Prenatal diagnosis.

Trisomy 20 mosaicism caused by a maternal meiosis II error is associated with normal intellect but multiple congenital anomalies

J. Ellison, D. Dawson, S. Jalal, 2005, American journal of medical genetics. Part A.

Primary body cavity-based AIDS-related lymphomas.

L. Picker, D. Dawson, M. Ansari, 1996, American journal of clinical pathology.

Large cell lymphoma transformation of chronic lymphocytic leukemia/small lymphocytic lymphoma. A flow cytometric analysis of seven cases.

D. Dawson, S. Kroft, R. Mckenna, 2001, American journal of clinical pathology.

Precursor B-lymphoblastic transformation of grade I follicle center lymphoma.

C. Ross, D. Dawson, T. Singleton, 2000, American journal of clinical pathology.

Assignment of the human peroxisomal palmitoyl-CoA oxidase gene to chromosome 17q23-qter by PCR technique

D. Dawson, M. Bennett, N. Moghrabi, 1995, Journal of Inherited Metabolic Disease.

Polymerase chain reaction amplification of archival material for Epstein-Barr virus, cytomegalovirus, human herpesvirus 6, and parvovirus B19 in children with bone marrow hemophagocytosis.

R. Scheuermann, D. Dawson, M. Hoang, 1998, Human pathology.

Comprehensive mutation screening in 55 probands with type 1 primary hyperoxaluria shows feasibility of a gene-based diagnosis.

D. Dawson, P. Lundquist, P. Harris, 2007, Journal of the American Society of Nephrology : JASN.

Central diabetes insipidus in a patient with NFKB2 mutation: Expanding the endocrine phenotype in DAVID syndrome.

Cassandra Brady, D. Dawson, D. Neilson, 2019, The Journal of clinical endocrinology and metabolism.

Immunophenotypic analysis of peripheral T-cell neoplasms. A multiparameter flow cytometric approach.

L. Picker, D. Dawson, S. Kroft, 2001, American journal of clinical pathology.

Carrier identification of cystic fibrosis by recombinant DNA techniques.

D. Schaid, S. Thibodeau, D. Dawson, 1989, Mayo Clinic proceedings.

Subspecialty Clinics: Medical Genetics Carrier Identification of Cystic Fibrosis by Recombinant

D. Schaid, S. Thibodeau, D. Dawson, 1989 .

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.

D. Dawson, P. Lundquist, W. Highsmith, 2011, The Journal of molecular diagnostics : JMD.

Assignment of the human peroxisomal branched-chain acyl-CoA oxidase gene to chromosome 3p21.1-p14.2 by rodent/human somatic cell hybridization.

S. Naylor, D. Dawson, M. Bennett, 1997, Biochemical and biophysical research communications.

Patients with mosaic methylation patterns of the Prader-Willi/Angelman Syndrome critical region exhibit AS-like phenotypes with some PWS features

E. Thorland, D. Dawson, N. Hoppman, 2016, Molecular Cytogenetics.

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)

Michael J. Donnelly, D. Dawson, J. Hoyer, 2014, Hemoglobin.

Characterization of Reference Materials for CYP2C9, CYP2C19, VKORC1, CYP2C Cluster Variant, GGCX, and Other Pharmacogenetic Alleles with an Association for Molecular Pathology (AMP) Pharmacogenetics Working Group Tier 2 Status - A GeT-RM Collaborative Project.

U. Broeckel, D. Dawson, A. Gaedigk, 2021, The Journal of molecular diagnostics : JMD.

FOUR NEW β CHAIN HEMOGLOBIN VARIANTS WITHOUT CLINICAL OR HEMATOLOGICAL EFFECTS: Hb SAN BRUNO [β39(C5)Gln→His]; Hb FORT DODGE [β93(F9)Cys→Tyr]; Hb RHODE ISLAND [β116(G18)His→Tyr]; AND Hb INGLEWOOD [β142(H20)Ala→Thr]

D. Dawson, J. Hoyer, K. Snow, 2002 .

Immunophenotypic analysis of peripheral T-cell neoplasms. A multiparameter flow cytometric approach.

L. Picker, D. Dawson, S. Kroft, 2001, American journal of clinical pathology.

Diagnosis of alpha-1-antitrypsin deficiency: An algorithm of quantification, genotyping, and phenotyping.

S. Thibodeau, J. Katzmann, D. Dawson, 2006, Clinical chemistry.