Comparative genomic hybridization of 49 primary retinoblastoma tumors identifies chromosomal regions associated with histopathology, progression, and patient outcome. (Q44267056)

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English	Comparative genomic hybridization of 49 primary retinoblastoma tumors identifies chromosomal regions associated with histopathology, progression, and patient outcome.	scientific article

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12508240%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

Comparative genomic hybridization of 49 primary retinoblastoma tumors identifies chromosomal regions associated with histopathology, progression, and patient outcome (English)

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16 December 2019

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8

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16 December 2019

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Debra M Lillington

1

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16 December 2019

Judith E Kingston

2

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16 December 2019

Pietro G Coen

3

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16 December 2019

Elizabeth Price

4

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16 December 2019

John Hungerford

5

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16 December 2019

Paola Domizio

6

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16 December 2019

Bryan D Young

7

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16 December 2019

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1 February 2003

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16 December 2019

Genes, Chromosomes and Cancer

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16 December 2019

36

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16 December 2019

2

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16 December 2019

121-128

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16 December 2019

Nonrandom chromosomal changes in untreated retinoblastomas

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Cytogenetic findings in 73 osteosarcoma specimens and a review of the literature

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Minimal regions of chromosomal imbalance in retinoblastoma detected by comparative genomic hybridization

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A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

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Structural evidence for the authenticity of the human retinoblastoma gene

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Overview of RB gene mutations in patients with retinoblastoma. Implications for clinical genetic screening

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Marked differences in unilateral isolated retinoblastomas from young and older children studied by comparative genomic hybridization

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Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors

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Proliferation not apoptosis as a prognostic indicator in retinoblastoma

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Mutation and cancer: statistical study of retinoblastoma

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Genetics and the Etiology of Childhood Cancer

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Mice deficient for Rb are nonviable and show defects in neurogenesis and haematopoiesis

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High level amplification of N-MYC is not associated with adverse histology or outcome in primary retinoblastoma tumours

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Detection of chromosome imbalances in retinoblastoma by parallel karyotype and CGH analyses

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Clinical importance of cytogenetics in acute myeloid leukaemia

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The retinoblastoma gene family: cousins with overlapping interests

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Chromosome evolution in retinoblastoma

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Incidence of second neoplasms in patients with bilateral retinoblastoma

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Molecular and cytologic analysis of DNA amplification in retinoblastoma

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Fluorescence in situ hybridization techniques for the rapid detection of genetic prognostic factors in neuroblastoma. United Kingdom Children's Cancer Study Group

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Retinoblastoma in transgenic mice

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