Reassessment of an apparent t(12;17)(p11;p11) as an unbalanced t(17;21)(p11;q11) in a case of B-cell chronic lymphocytic leukemia by fluorescence in situ hybridization

Author:

Flactif Martial,Luc Laï Jean,Fenaux Pierre

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

Reference18 articles.

1. Mutations of the P53 gene in B-cell chronic lymphocytic leukemia: A report on 39 cases with cytogenetic analysis;Fenaux;Leukemia,1992

2. Molecular Cloning: A Laboratory Manual;Sambrook,1989

3. Rapid detection of human chromosome 21 aberrations by in situ hybridization;Lichter,1988

4. Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries;Lichter;Hum Genet,1988

5. Fluorescence in situ hybridization with human chromosome-specific libraries: Detection of trisomy 21 and translocations of chromosome 4;Pinkel,1988

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