The Journal of molecular diagnostics

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  Año 2004, Vol. 6, Número 4

  • Hereditary non-syndromic sensorineural hearing loss: transforming silence to sound

    Iris Schrijver

    págs. 275-284

    

  • Triplet repeat primed PCR (TP PCR) in molecular diagnostic testing for Friedreich ataxia

    F. Ajmar, P. Mandich, P. Ciotti, E. Di Maria, E. Bellone

    págs. 285-289

    

  • RT-PCR analysis of RNA extracted from bouin-fixed and paraffin-embedded lymphoid tissues

    L. Dal Maso, Tiziana Perin, R. Dalla Favera, Antonino Carbone, Annunziata Gloghini, B. Canal, U. Klein

    págs. 290-296

    

  • Constitutive expression of the AP-1 transcription factors c-jun, junD, junB, and c-fos and the marginal zone B-cell transcription factor Notch2 in splenic marginal zone lymphoma

    I. M. Ikonomou, A. Tierens, E. Matutes, A. Gruszka Westwood, D. Catovsky, O. Myklebost, G. Lauritzsen, E. Hovig, J. Delabie, G. Trøen, V. Nygaard, T. Jenssen

    págs. 297-307

    

  • Challenges and pitfalls in HNPCC screening by microsatellite analysis and immunohistochemistry

    M. Mathiak, B. Roggendorf, E. Heinmöller, T. Brodegger, G. Tuccari , Elisabeth Mangold , R. Buettner, Jan H. Rüschoff, Deutsche Krebshilfe , German HNPCC Consortium , German Cancer Aid , A. Müller, G. Giuffre, T. B. Edmonston

    págs. 308-315

    

  • Intratumoral patterns of clonal evolution in meningiomas as defined by multicolor interphase fluorescence in situ hybridization (FISH): Is there a relationship between histopathologically benign and atypical/anaplastic lesions?

    A. Espinosa, A. Rasillo, P. Díaz, J. Ciudad, A. López, M. Merino, Jesús María Gonçalves, Ángel Santos-Briz Terrón, F. Morales, Alberto Orfao, José M. Sayagues Manzano, María Dolores Tabernero, A. Maíllo

    págs. 316-325

    

  • Promoter hypermethylation of multiple genes in hydatidiform mole and choriocarcinoma

    P. Chiu, H. Y. Ngan, S. Tsao, A. N. Cheung, W. Xue, K. Y. Chan, H. Feng

    págs. 326-334

    

  • Demonstration that mast cells, T Cells, and B Cells bearing the activating kit mutation D816V occur in clusters within the marrow of patients with mastocytosis

    H. Obiakor, C. Akin, R. G. Mage, D. D. Metcalfe, M. L. Taylor, D. Sehgal, M. Raffeld

    págs. 335-342

    

  • Characterization of the different BCR-ABL transcripts with a single multiplex RT-PCR

    J. C. Chomel, Francesco Guidi, N. Bourmeyster, Alain Kitzis Jacques, J. Rivet, F. Bilan, J. Chasseriau

    págs. 343-347

    

  • Microsphere bead arrays and sequence validation of 5/7/9T genotypes for multiplex screening of cystic fibrosis polymorphisms

    M. R. Badgett, L. A. Isgur, M. Goldrick, C. R. WalkerPeach, Andrew G. Hadd, W. Laosinchai Wolf, C. R. Novak

    págs. 348-355

    

  • Measurement of relative copy number of CDKN2A/ARF and CDKN2B in bladder cancer by real-time quantitative PCR and multiplex ligation-dependent probe amplification

    J. S. Aveyard, M. A. Knowles

    págs. 356-365

    

  • KIT Gene deletions at the intron 10-Exon 11 boundary in GI stromal tumors

    A. Schroeder, Troy Bainbridge, Patina Harrell, J. A. Fletcher, M. C. Heinrich, Christopher L. Corless, L. McGreevey, A. Town

    págs. 366-370

    

  • Comparison of snap freezing versus ethanol fixation for gene expression profiling of tissue specimens

    Y. Gathright, Sergio González, Alfredo Velasco, W. M. Linehan, Michael R. Emmert Buck, Rodrigo F. Chuaqui, M. A. Perlmutter, C. J. Best, John W. Gillespie

    págs. 371-377

    

  • Epstein-barr virus quantitation by real-time PCR targeting multiple gene segments: a novel approach to screen for the virus in paraffin-embedded tissue and plasma

    S. A. Schichman, N. Raab Traub, Margaret L. Gulley, J. L. Ryan, Hongxin Fan, S. L. Glaser

    págs. 378-385

    

  • Enhanced retrieval of DNA from human fecal samples results in improved performance of colorectal cancer screening test

    K. Boynton, L. Kann, R. Brand, S. Syngal, M. Lawson, A. Shuber, D. Whitney, J. Skoletsky, K. Moore

    págs. 386-395

    

  • Quantitative PCR detection of t(14;18) bcl-2/JH fusion sequences in follicular lymphoma patients: comparison of peripheral blood and bone marrow aspirate samples

    R. Luthra, A. Bowman, Dan Jones, L. Jeffrey Medeiros

    págs. 396-400

    

  • A rare mutation in the primer binding region of the amelogenin gene can interfere with gender identification

    I. Warshawsky, B. Shadrach, M. Commane, C. Hren

    págs. 401-405

    

  • Association for molecular pathology 2004 annual meeting abstracts

    págs. 406-439