Specificity of interphase fluorescence in situ hybridization for detection of chromosome aberrations in tumor pathology

Cancer Genetics and Cytogenetics

Volumn 155, Issue 2, 2004, Pages 143-148

  Tibiletti, M G ^a  

^a OSPEDALE DI CIRCOLO   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

PARAFFIN;

ARTICLE; CANCER DIAGNOSIS; CANCER GENETICS; CELL NUCLEUS; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CLINICAL ARTICLE; CONTROLLED STUDY; CYTOGENETICS; DIAGNOSTIC ACCURACY; DIAGNOSTIC PROCEDURE; FLUORESCENCE IN SITU HYBRIDIZATION; FROZEN SECTION; HISTOCHEMISTRY; HISTOPATHOLOGY; HUMAN; HUMAN CELL; HUMAN TISSUE; INTERPHASE FLUORESCENCE IN SITU HYBRIDIZATION; MOLECULAR CLONING; MOLECULAR PROBE; MONOSOMY; PRIORITY JOURNAL; SENSITIVITY ANALYSIS; TRISOMY;

BONE MARROW; CELL NUCLEUS; CHROMOSOME ABERRATIONS; CODON, NONSENSE; DIAGNOSTIC ERRORS; DNA PROBES; FRAMESHIFT MUTATION; GENE DELETION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MONOSOMY; NEOPLASMS; SENSITIVITY AND SPECIFICITY; TRISOMY;

EID: 9644302423     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2004.03.005     Document Type: Article

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