Detection by fluorescence in situ hybridization of microdeletions at 1p36 in lymphomas, unidentified on cytogenetic analysis (Q56459382)

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1 November 2019

title

Detection by fluorescence in situ hybridization of microdeletions at 1p36 in lymphomas, unidentified on cytogenetic analysis (English)

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1 November 2019

8

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1 November 2019

author name string

Achuthan Rajgopal

1

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1 November 2019

Donald Hodge

4

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1 November 2019

Paul Roberts

6

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1 November 2019

Kieran Horgan

7

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1 November 2019

Ian M Carr

2

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1 November 2019

Jack P Leek

3

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1 November 2019

Sandra M Bell

5

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1 November 2019

Peter J Selby

9

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1 November 2019

Alexander F Markham

10

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1 November 2019

Kenneth A MacLennan

11

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1 November 2019

publication date

1 April 2003

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Cancer Genetics and Cytogenetics

1 November 2019

published in

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volume

142

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issue

1

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page(s)

46-50

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describes a project that uses

1 November 2019

fluorescence in situ hybridization

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Loss of heterozygosity at chromosome 1p in different solid human tumours: association with survival

inferred from title

cites work

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7 January 2021

Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: correlation with N-myc amplification

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7 January 2021

Frequent allelic imbalance suggests involvement of a tumor suppressor gene at 1p36 in the pathogenesis of human lung cancers

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7 January 2021

Characterization of chromosome 1 abnormalities in malignant melanomas

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7 January 2021

Allele loss on chromosome 1p36 in epithelial ovarian cancers

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7 January 2021

Chromosomes 1 and 12 abnormalities in pediatric germ cell tumors by interphase fluorescence in situ hybridization

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7 January 2021

Refined chromosomal localization of the putative tumor suppressor gene TP73.

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7 January 2021

Abnormalities in the p34cdc2-related PITSLRE protein kinase gene complex (CDC2L) on chromosome band 1p36 in melanoma

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7 January 2021

Causal relationship between the loss of RUNX3 expression and gastric cancer

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7 January 2021

Novel translocation of the BCL10 gene in a case of mucosa associated lymphoid tissue lymphoma.

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7 January 2021

A breakpoint map of recurrent chromosomal rearrangements in human neoplasia

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7 January 2021

Terminal deletion, del(1)(p36.3), detected through screening for terminal deletions in patients with unclassified malformation syndromes.

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7 January 2021

Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes.

1 reference

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7 January 2021

10.1016/S0165-4608(02)00740-9

Identifiers

DOI

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1 November 2019

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