Risk of false positive results in comparative genomic hybridization

Genes Chromosomes and Cancer

Volumn 28, Issue 3, 2000, Pages 353-357

  Barth, Thomas F E ^a   Benner, Axel ^b   Bentz, Martin ^c   Döhner, Hartmut ^c   Möller, Peter ^a   Lichter, Peter ^b  

^a UNIVERSITY OF ULM   (Germany)

^b GERMAN CANCER RESEARCH CENTER DKFZ   (Germany)

^c UNIVERSITY HOSPITAL ULM   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; B CELL LYMPHOMA; CHROMOSOME ABERRATION; CHROMOSOME MAP; CHRONIC LYMPHATIC LEUKEMIA; COMPARATIVE GENOMIC HYBRIDIZATION; DIAGNOSTIC ACCURACY; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC SCREENING; HUMAN; HUMAN TISSUE; MANTLE CELL LYMPHOMA; PRIORITY JOURNAL;

CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; FALSE POSITIVE REACTIONS; GENOMIC LIBRARY; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LEUKEMIA, LYMPHOCYTIC, CHRONIC; LYMPHOMA, B-CELL; NUCLEIC ACID HYBRIDIZATION; PREDICTIVE VALUE OF TESTS; RISK FACTORS;

EID: 0034043242     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/1098-2264(200007)28:3<353::AID-GCC15>3.0.CO;2-0     Document Type: Article

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