(Q55480598)

12 July 2018

title

Molecular analysis of genetic changes in ependymomas. (English)

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12 July 2018

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Bijlsma EK

1

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12 July 2018

Voesten AM

2

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12 July 2018

Bijleveld EH

3

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12 July 2018

Troost D

4

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12 July 2018

Westerveld A

5

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12 July 2018

Mérel P

6

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12 July 2018

Thomas G

7

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12 July 2018

Hulsebos TJ

8

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12 July 2018

publication date

1 August 1995

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12 July 2018

Genes, Chromosomes and Cancer

published in

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12 July 2018

volume

13

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12 July 2018

issue

4

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12 July 2018

page(s)

272-277

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12 July 2018

Evidence of allelic imbalance of chromosome 6 in human astrocytomas.

cites work

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130407

Multiple sequential molecular abnormalities in the evolution of human gliomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130407

Molecular analysis of chromosome 1 abnormalities in human gliomas reveals frequent loss of 1p in oligodendroglial tumors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130407

7 January 2021

Gene and chromosomal alterations associated with the development of human gliomas.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130407

7 January 2021

Deletion mapping of a locus on human chromosome 22 involved in the oncogenesis of meningioma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130407

7 January 2021

The 1993-94 Généthon human genetic linkage map

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130407

7 January 2021

p53 mutations in human cancers

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130407

7 January 2021

Loss of genetic information in central nervous system tumors common to children and young adults.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130407

7 January 2021

Loss of heterozygosity in malignant gliomas involves at least three distinct regions on chromosome 10.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130407

7 January 2021

Neurofibromatosis 2 (bilateral acoustic neurofibromatosis).

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130407

7 January 2021

Cytogenetic analysis of 109 pediatric central nervous system tumors.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130407

7 January 2021

Cytogenetic and loss of heterozygosity studies in ependymomas, pilocytic astrocytomas, and oligodendrogliomas

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130407

7 January 2021

Abnormalities of chromosome 22 in human brain tumors determined by combined cytogenetic and molecular genetic approaches.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130407

7 January 2021

Chromosome aberrations in four ependymomas

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130407

7 January 2021

Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130407

7 January 2021

MTS1/CDKN2 gene mutations are rare in primary human astrocytomas with allelic loss of chromosome 9p

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130407

7 January 2021

Identifiers

DOI

10.1002/GCC.2870130407

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12 July 2018

PubMed ID

7547635

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12 July 2018