(Q55474890)

English

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

scientific article published in October 2000

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scholarly article

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/11104027

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

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/11104027

author name string

Zheng PP

1

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/11104027

Pang JC

2

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/11104027

Hui AB

3

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/11104027

Ng HK

4

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/11104027

publication date

1 October 2000

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/11104027

number of pages

8

1 reference

based on heuristic

inferred from page(s)

Cancer Genetics and Cytogenetics

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Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/11104027

122

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Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/11104027

18-25

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Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/11104027

1

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/11104027

The molecular biology of ependymomas

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The new WHO classification of brain tumours

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Prognostic relevance of localization and grading in intracranial ependymomas of childhood.

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Intracranial ependymomas of childhood. Lack of correlation of histopathology and clinical outcome.

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Chromosome abnormalities in low-grade central nervous system tumors

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Chromosomes in the genesis and progression of ependymomas.

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

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Detection of chromosomal imbalances in growth hormone-secreting pituitary tumors by comparative genomic hybridization

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Exon scanning for mutations of the NF2 gene in pediatric ependymomas, rhabdoid tumors and meningiomas

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

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Chromosome aberrations in four ependymomas

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Multiple chromosome rearrangements in a childhood ependymoma

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Construction of a high-resolution physical and transcription map of chromosome 16q24.3: a region of frequent loss of heterozygosity in sporadic breast cancer.

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Identification of a germ-line mutation in the p53 gene in a patient with an intracranial ependymoma

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Allelic loss on chromosome 6Q in primary prostate cancer

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Suppression of tumorigenicity in human ovarian cancer cell lines is controlled by a 2 cM fragment in chromosomal region 6q24-q25.

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Comparative genomic hybridization studies in hydatidiform moles and choriocarcinoma: amplification of 7q21-q31 and loss of 8p12-p21 in choriocarcinoma.

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Identifiers

10.1016/S0165-4608(00)00265-X

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/11104027

1 reference

Europe PubMed Central

12 July 2018

http://europepmc.org/abstract/MED/11104027

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