Michael J. Hafez

发表

[Clinicopathological features and types of microsatellite instability in 1394 patients with colorectal cancer].

Kathleen M Murphy, Michael J Hafez, Shengle Zhang, 2020, Nan fang yi ke da xue xue bao = Journal of Southern Medical University.

Detection of FLT3 internal tandem duplication and D835 mutations by a multiplex polymerase chain reaction and capillary electrophoresis assay.

K. Murphy, B. Smith, M. Levis, 2003, The Journal of molecular diagnostics : JMD.

Δ-PCR, A Simple Method to Detect Translocations and Insertion/Deletion Mutations.

J. Eshleman, Ming-Tseh Lin, K. Murphy, 2011, The Journal of molecular diagnostics : JMD.

Diagnosis and subclassification of hydatidiform moles utilizing p57 immunohistochemistry and molecular genotyping: Validation and prospective analysis in routine and consultation practice settings with development of an algorithmic approach (American Journal of Surgical Pathology (2009) 33, (805-817

K. Murphy, T. McConnell, M. Hafez, 2009 .

Performance and clinical evaluation of a sensitive multiplex assay for the rapid detection of common NPM1 mutations.

Keith D Jackson, J. Karp, E. Labourier, 2010, The Journal of molecular diagnostics : JMD.

Genetic variation in DNA-repair pathways and response to radiochemotherapy in esophageal adenocarcinoma: a retrospective cohort study of the Eastern Cooperative Oncology Group

E. Montgomery, P. Catalano, Xifeng Wu, 2011, BMC Cancer.

Comparison of Sanger sequencing, pyrosequencing, and melting curve analysis for the detection of KRAS mutations: diagnostic and clinical implications.

Kathleen M Murphy, Michael J Hafez, Christopher D Gocke, 2010, The Journal of molecular diagnostics : JMD.

Liquid bead array technology in the detection of common translocations in acute and chronic leukemias.

Rodney E Shackelford, Keith D Jackson, Michael J Hafez, 2013, Methods in molecular biology.

Little or No Residual Prostate Cancer at Radical Prostatectomy: Vanishing Cancer or Switched Specimen?: A Microsatellite Analysis of Specimen Identity

J. Epstein, K. Murphy, D. Cao, 2005, The American journal of surgical pathology.

Molecular genotyping of hydatidiform moles: analytic validation of a multiplex short tandem repeat assay.

K. Murphy, T. McConnell, M. Hafez, 2009, The Journal of molecular diagnostics : JMD.

Diagnosis and Subclassification of Hydatidiform Moles Using p57 Immunohistochemistry and Molecular Genotyping: Validation and Prospective Analysis in Routine and Consultation Practice Settings With Development of an Algorithmic Approach

K. Murphy, T. McConnell, M. Hafez, 2009, The American journal of surgical pathology.

Evaluation of Temperature Gradient Capillary Electrophoresis for Detection of the Factor V Leiden Mutation

K. Murphy, J. Philips, M. Hafez, 2012, Molecular Diagnosis.

Performance and clinical evaluation of a sensitive multiplex assay for the rapid detection of common NPM1 mutations.

Keith D Jackson, J. Karp, E. Labourier, 2010, The Journal of molecular diagnostics : JMD.

Consultations in Molecular Diagnostics Capillary Electrophoresis Artifact Due to Eosin Implications for the Interpretation of Molecular Diagnostic Assays

J. Eshleman, K. Murphy, Katie A. Flickinger, 2005 .

Lack of a Y-Chromosomal Complement in the Majority of Gestational Trophoblastic Neoplasms

I. Shih, R. Kurman, K. Murphy, 2010, Journal of oncology.

A single nucleotide primer extension assay to detect the APC I1307K gene variant.

J. Eshleman, K. Murphy, C. Griffin, 2003, The Journal of molecular diagnostics : JMD.