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Clinical Chemistry|October 1, 1996
Dynamic mutations pose unique challenges for the molecular diagnostics laboratoryR C McGlennenClinical Chemistry|March 10, 2001
Miniaturization technologies for molecular diagnosticsR C McGlennenMethods in Molecular Medicine|March 4, 2011
Methods to detect clonal gene rearrangements in lymphomas and leukemiasN Mitha, R C McGlennenMethods in Molecular Medicine|March 4, 2011
Monitoring of bone marrow transplant engraftmentK P Woronzoff-Dashkoff, R C McGlennenMolecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology|September 26, 2001
Simultaneous allele-specific amplification: a strategy using modified primer-template mismatches for SNP detection--application to prothrombin 20210A (factor II) and factor V Leiden (1691A) gene mutationsS A DelRio-LaFreniere, R C McGlennenCancer Research|October 1, 1994
Clonal determination by the fragile X (FMR1) and phosphoglycerate kinase (PGK) genes in hematological malignanciesS T Lee, R C McGlennen, C E LitzArchives of Pathology & Laboratory Medicine|October 1, 1986
Systemic amyloidosis complicating cystic fibrosis. A retrospective pathologic studyR C McGlennen, B A Burke, L P DehnerArchives of Neurology|May 18, 2000
Hereditary spastic paraplegia and hereditary ataxia, Part 2: A family demonstrating various phenotypic manifestations with the SCA3 genotypeW M Landau, R E Schmidt, R C McGlennen, et al.The American Journal of Pathology|February 1, 1986
Adrenocortical carcinoma. An immunohistochemical comparison with renal cell carcinomaM R Wick, D L Cherwitz, R C McGlennen, et al.Pageof 4