Minimal regions of chromosomal imbalance in retinoblastoma detected by comparative genomic hybridization (Q57791050)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11520568%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

title

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

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10 November 2019

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1

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10 November 2019

Brenda L. Gallie

series ordinal

2

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10 November 2019

Jeremy A. Squire

series ordinal

3

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10 November 2019

publication date

1 August 2001

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Cancer Genetics and Cytogenetics

10 November 2019

published in

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10 November 2019

volume

129

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10 November 2019

issue

1

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10 November 2019

page(s)

57-63

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Mutation and cancer: statistical study of retinoblastoma

10 November 2019

cites work

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Isochromosome 6p, a unique chromosomal abnormality in retinoblastoma: Verification by standard staining techniques, new densitometric methods, and somatic cell hybridization

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

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Chromosomal abnormalities in human retinoblastoma. A review

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Expression and amplification of the N-myc gene in primary retinoblastoma

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Genetic instability in colorectal cancers

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Significance of Retinoma and Phthisis Bulbi for Retinoblastoma

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Retinoma: spontaneous regression of retinoblastoma or benign manifestation of the mutation?

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Distinct roles for E2F proteins in cell growth control and apoptosis

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Molecular Genetic Studies of Tumor suppressor Gene Regions on chromosomes 13 and 17 in Colorectal Tumors

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Expression of the E2F family in human gastrointestinal carcinomas

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Replicative senescence, aging and growth-regulatory transcription factors

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N-MYC amplification, loss of heterozygosity on the short arm of chromosome 1 and DNA ploidy in retinoblastoma

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10.1016/S0165-4608(01)00427-7

Identifiers

DOI

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10 November 2019

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