(Q60212965)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7504513%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

title

Three non-overlapping regions of chromosome arm 11p allele loss identified in infantile tumors of adrenal and liver (English)

1 reference

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19 October 2019

3

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19 October 2019

author name string

Byrne JA

1

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19 October 2019

Simms LA

2

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19 October 2019

Algar EM

4

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19 October 2019

Smith PJ

5

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19 October 2019

publication date

1 October 1993

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Genes, Chromosomes and Cancer

19 October 2019

published in

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19 October 2019

volume

8

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19 October 2019

page(s)

104-111

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19 October 2019

issue

2

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Reduction to homozygosity of genes on chromosome 11 in human breast neoplasia

19 October 2019

cites work

1 reference

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7 January 2021

Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome

1 reference

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7 January 2021

Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development

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7 January 2021

SacI polymorphism in the RRM1 gene

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7 January 2021

The M1 subunit of ribonucleotide reductase refines mapping of genetic rearrangements at chromosome 11p15.

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7 January 2021

Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus

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7 January 2021

A comprehensive and critical assessment of overgrowth and overgrowth syndromes

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7 January 2021

Suppression of tumorigenicity in Wilms tumor by the p15.5-p14 region of chromosome 11.

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7 January 2021

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

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7 January 2021

"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum

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7 January 2021

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

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7 January 2021

Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11.

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7 January 2021

Alternative splicing and genomic structure of the Wilms tumor gene WT1

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7 January 2021

Generation of homozygosity at the c-Ha-ras-1 locus on chromosome 11p in an adrenal adenoma from an adult with Wiedemann—Beckwith syndrome

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7 January 2021

Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma

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7 January 2021

Lack of linkage of familial Wilms' tumour to chromosomal band 11 p13

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7 January 2021

Beckwith-Wiedemann syndrome, tumourigenesis and imprinting

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7 January 2021

Report of the committee on the genetic constitution of chromosome 11

1 reference

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7 January 2021

Report of the Second Chromosome 11 Workshop

1 reference

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7 January 2021

Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080207

7 January 2021

Loss of alleles on the short arm of chromosome 11 in a hepatoblastoma from a child with Beckwith-Wiedemann syndrome.

1 reference

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7 January 2021

Allelic loss on chromosome 11p is a less frequent event in bilateral than in unilateral Wilms' tumours

1 reference

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7 January 2021

Zinc finger point mutations within the WT1 gene in Wilms tumor patients

1 reference

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7 January 2021

Partial deletion of chromosome 11p in breast cancer correlates with size of primary tumour and oestrogen receptor level

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https://api.crossref.org/works/10.1002%2FGCC.2870080207

7 January 2021

Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours

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7 January 2021

WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080207

7 January 2021

Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080207

7 January 2021

The candidate Wilms' tumour gene is involved in genitourinary development

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080207

7 January 2021

Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080207

7 January 2021

Direct pulsed field gel electrophoresis of Wilms' tumors shows that dna deletions in 11 p 13 are rare

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080207

7 January 2021

Familial predisposition to Wilms tumor does not segregate with the WT1 gene.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080207

7 January 2021

Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080207

7 January 2021

A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080207

7 January 2021

Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870080207

7 January 2021

Identifiers

DOI

10.1002/GCC.2870080207

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7504513%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

1 reference