Fluorescence in situ hybridization determination of 22q12-q13 deletion in two intracerebral ependymomas. (Q55474979)

12 July 2018

title

Fluorescence in situ hybridization determination of 22q12-q13 deletion in two intracerebral ependymomas. (English)

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12 July 2018

author name string

Rousseau-Merck M

1

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12 July 2018

Versteege I

2

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12 July 2018

Zattara-Cannoni H

3

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12 July 2018

Figarella D

4

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12 July 2018

Lena G

5

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12 July 2018

Aurias A

6

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12 July 2018

Vagner-Capodano AM

7

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12 July 2018

publication date

1 September 2000

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12 July 2018

Cancer Genetics and Cytogenetics

published in

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12 July 2018

volume

121

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12 July 2018

issue

2

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12 July 2018

page(s)

223-227

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12 July 2018

Chromosomal abnormalities in 47 pediatric brain tumors

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Cytogenetic analysis of 120 primary pediatric brain tumors and literature review

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Cytogenetic findings in a supratentorial ependymoma

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Recurrent anaplastic ependymoma with an abnormal karyotype and c-myc proto-oncogene overexpression.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

A cytogenetic study of 53 human gliomas.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Cytogenetic analysis of 109 pediatric central nervous system tumors.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Cytogenetics of pediatric central nervous system tumors.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Chromosome aberrations in four ependymomas

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Clonal telomeric fusions and chromosome instability in a subcutaneous sacrococcygeal myxopapillary ependymoma.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Chromosome analysis of brain tumors in childhood

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Molecular cytogenetic studies of pediatric ependymomas

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Familial anaplastic ependymoma: evidence of loss of chromosome 22 in tumour cells

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Chromosomes in the genesis and progression of ependymomas.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Constitutional de novo t(1;22)(p22;q11.2) and ependymoma.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Cytogenetic studies in 45 pediatric brain tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Cytogenetic study of 33 ependymomas.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Cytogenetic evidence for a chromosome 22 tumor suppressor gene in ependymoma

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Involvement of chromosome 22 in ependymomas.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Karyotype studies in 18 ependymomas with literature review of 107 cases

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Cytogenetic abnormalities in human ependymomas.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Chromosome studies in 70 brain tumors with special attention to sex chromosome loss and single autosomal trisomy.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Cloning and characterization of the Ewing's sarcoma and peripheral neuroepithelioma t(11;22) translocation breakpoints

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Localization of 27 DNA markers to the region of human chromosome 22q11-pter deleted in patients with the DiGeorge syndrome and duplicated in the der22 syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Assignment of the human stromelysin 3 (STMY3) gene to the q11.2 region of chromosome 22

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Predominant occurrence of somatic mutations of theNF2 gene in meningiomas and schwannomas

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Molecular genetic analysis of ependymal tumors. NF2 mutations and chromosome 22q loss occur preferentially in intramedullary spinal ependymomas

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Spectrum of hSNF5/INI1 somatic mutations in human cancer and genotype-phenotype correlations

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

The molecular biology of ependymomas

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Chromosome arm 6q loss is the most common recurrent autosomal alteration detected in primary pediatric ependymoma

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Molecular studies of an ependymoma-associated constitutional t(1;22)(p22;q11.2).

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Neurofibromatosis 2 (bilateral acoustic neurofibromatosis).

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

Frequent type 2 neurofibromatosis gene transcript mutations in sporadic intramedullary spinal cord ependymomas

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

The DNA sequence of human chromosome 22

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900262-4

7 January 2021

10.1016/S0165-4608(00)00262-4

Identifiers

DOI

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12 July 2018

PubMed ID

11063814

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12 July 2018