(Q48736287)

15 February 2018

title

Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogenetics. (English)

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15 February 2018

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Granzow M

1

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15 February 2018

Popp S

2

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15 February 2018

Weber S

3

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15 February 2018

Schoell B

4

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15 February 2018

Holtgreve-Grez H

5

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15 February 2018

Senf L

6

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15 February 2018

Hager D

7

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15 February 2018

Boschert J

8

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15 February 2018

Scheurlen W

9

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15 February 2018

Jauch A

10

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15 February 2018

publication date

1 October 2001

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15 February 2018

Cancer Genetics and Cytogenetics

published in

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15 February 2018

volume

130

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15 February 2018

issue

1

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15 February 2018

page(s)

79-83

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15 February 2018

cites work

Brain tumors in children

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900465-4

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%2801%2900465-4

7 January 2021

Chromosomes in the genesis and progression of ependymomas.

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https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900465-4

7 January 2021

Involvement of chromosome 22 in ependymomas.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900465-4

7 January 2021

Molecular cytogenetic studies of pediatric ependymomas

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900465-4

7 January 2021

Evidence for an ependymoma tumour suppressor gene in chromosome region 22pter-22q11.2.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900465-4

7 January 2021

Cytogenetic study of 33 ependymomas.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900465-4

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%2801%2900465-4

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%2801%2900465-4

7 January 2021

An optimized, fully automated system for fast and accurate identification of chromosomal rearrangements by multiplex-FISH (M-FISH).

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900465-4

7 January 2021

Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization.

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https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900465-4

7 January 2021

Rapid generation of region specific probes by chromosome microdissection and their application

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https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900465-4

7 January 2021

Cytogenetic analysis of 109 pediatric central nervous system tumors.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900465-4

7 January 2021

Isochromosomes in neoplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900465-4

7 January 2021

Comparative genomic hybridization detects losses of chromosomes 22 and 16 as the most common recurrent genetic alterations in primary ependymomas.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900465-4

7 January 2021

DNA copy number losses in human neoplasms

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900465-4

7 January 2021

Cytogenetic abnormalities in human ependymomas.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900465-4

7 January 2021

Molecular analysis of genetic changes in ependymomas.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900465-4

7 January 2021

Infrequency of p53 gene mutations in ependymomas

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900465-4

7 January 2021

Mapping of the breakpoints on the short arm of chromosome 17 in neoplasms with an i(17q)

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900465-4

7 January 2021

10.1016/S0165-4608(01)00465-4

Identifiers

DOI

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15 February 2018

PubMed ID

11672779

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15 February 2018