A recurrent chondromyxoid fibroma with chromosome aberrations ins(5;2)(q13;p21p25) and 2p deletion: A case report-Reference-Cited by-同舟云学术

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A recurrent chondromyxoid fibroma with chromosome aberrations ins(5;2)(q13;p21p25) and 2p deletion: A case report

Published:1993-02 Issue:2 Volume:65 Page:141-146
ISSN:0165-4608
Container-title:Cancer Genetics and Cytogenetics
language:en
Short-container-title:Cancer Genetics and Cytogenetics

Author:

Tarkkanen Maija,Böhling Tom,Heliö Harri,Karaharju Erkki,Kaipainen Arja,Szymanska Jadwiga,Elomaa Inkeri,Knuutila Sakari

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

Reference16 articles.

1. Chondromyxoid fibroma;Huvos,1979

2. Chondromyxoid fibroma: Report of six cases with immunohistochemical studies;Bleiweiss;Mod Pathol,1990

3. Catalog of Chromosome Aberrations in Cancer;Mitelman,1991

4. Guidelines for cancer cytogenetics;ISCN,1991

5. Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization;Pinkel,1986

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1. Morphology Antibody Chromosome Technique for Determining Phenotype and Genetic Status of the Same Cell;Current Protocols in Human Genetics;2012-07

2. A t(1;9)(q10;q10) translocation with additional 6q23 and 9q22 rearrangements in a case of chondromyxoid fibroma;Cancer Genetics;2011-12

3. Aberrations of 6q13 mapped to the COL12A1 locus in chondromyxoid fibroma;Modern Pathology;2009-07-31

4. Juvenile juxtacortical chondromyxoid fibroma of bone: a case report;Human Pathology;2008-06

5. Chondromyxoid fibroma of rib with a novel chromosomal translocation: a report of four additional cases at unusual sites;Diagnostic Pathology;2007-11-24

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