Constitutional de novo t(1;22)(p22;q11.2) and ependymoma
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology
Reference13 articles.
1. Involvement of chromosome 22 in ependymomas;Wernicke;Cancer Genet Cytogenet,1995
2. Loss of genetic information in central nervous system tumors common to children and young adults;James;Genes Chromosom Cancer,1990
3. Chromosome abnormalities in low-grade central nervous system tumors;Griffin;Cancer Genet Cytogenet,1992
4. Cytogenetic and loss of heterozygosity studies in ependymomas, pilocytic astrocytomas, and oligodendrogliomas;Ransom;Genes Chromosom Cancer,1992
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1. De novo Unbalanced 1;22 Translocation with 22q11 Deletion Syndrome;Cytogenetic and Genome Research;2019
2. Ependymoma;Pediatric Oncology;2010
3. Loss of chromosome 1 in myxopapillary ependymoma suggests a region out of chromosome 22 as critical for tumour biology: a FISH analysis of four cases on touch imprint smears;Cytopathology;2006-08
4. Analysis of chromosome 7 in adult and pediatric ependymomas using chromogenic in situ hybridization;Journal of Neuro-Oncology;2005-03
5. A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2;Human Molecular Genetics;2004-01-01
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