Comparative genomic hybridization analysis identifies gains of 1p35∼p36 and chromosome 19 in osteosarcoma (Q57791017)

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13 November 2019

title

Comparative genomic hybridization analysis identifies gains of 1p35 approximately p36 and chromosome 19 in osteosarcoma (English)

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13 November 2019

10

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13 November 2019

author name string

M Zielenska

1

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13 November 2019

J Bayani

2

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13 November 2019

A Pandita

3

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13 November 2019

S Toledo

4

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13 November 2019

P Marrano

5

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13 November 2019

J Andrade

6

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13 November 2019

A Petrilli

7

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13 November 2019

P Thorner

8

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13 November 2019

P Sorensen

9

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13 November 2019

publication date

1 October 2001

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Cancer Genetics and Cytogenetics

13 November 2019

published in

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13 November 2019

volume

130

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13 November 2019

issue

1

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13 November 2019

page(s)

14-21

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Chromosome analysis of nine osteosarcomas

13 November 2019

cites work

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Cytogenetic aberrations in osteosarcomas. Nonrandom deletions, rings, and double-minute chromosomes

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Presence of double minutes and monosomy 17p in xenografted human osteosarcomas

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Radiation-associated sarcomas are characterized by complex karyotypes with frequent rearrangements of chromosome arm 3p

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DNA sequence copy number increase at 8q: a potential new prognostic marker in high-grade osteosarcoma

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Comparative genomic hybridization analysis of human sarcomas: II. Identification of novel amplicons at 6p and 17p in osteosarcomas

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Molecular cytogenetic analysis of medulloblastomas and supratentorial primitive neuroectodermal tumors by using conventional banding, comparative genomic hybridization, and spectral karyotyping.

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Multicolor Spectral Karyotyping of Human Chromosomes

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Lack of BCR/ABL reciprocal fusion in variant Philadelphia chromosome translocations: a use of double fusion signal FISH and spectral karyotyping

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Characterization of the 17p amplicon in human sarcomas: Microsatellite marker analysis

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Aberrations of chromosomes 1 and 17 in six human osteosarcoma cell lines using double-target fluorescence in situ hybridization

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Relationship between chromosomal aberrations by fluorescence in situ hybridization and DNA ploidy by cytofluorometry in osteosarcoma

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Specific genetic predictors of chemotherapeutic response and survival in patients with anaplastic oligodendrogliomas

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Prognostic impact of deletions at 1p36 and numerical aberrations in Ewing tumors

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Amplification of the MYCN oncogene and deletion of putative tumour suppressor gene in human neuroblastomas

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Identifiers

DOI

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13 November 2019

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