A constitutional BWS-related t(11;16) chromosome translocation occurring in the same region of chromosome 16 implicated in Wilms' tumors (Q71680196)

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20 October 2019

title

A constitutional BWS-related t(11;16) chromosome translocation occurring in the same region of chromosome 16 implicated in Wilms' tumors (English)

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20 October 2019

author name string

Newsham I

1

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20 October 2019

Kindler-Röhrborn A

2

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20 October 2019

Daub D

3

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20 October 2019

Cavenee W

4

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20 October 2019

publication date

1 January 1995

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Genes, Chromosomes and Cancer

20 October 2019

published in

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20 October 2019

volume

12

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20 October 2019

page(s)

1-7

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20 October 2019

issue

1

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An STS at the D16S290 locus

20 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870120102

7 January 2021

Loss of heterozygosity mapping in Wilms tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870120102

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870120102

7 January 2021

Parental-origin-specific epigenetic modification of the mouse H19 gene

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870120102

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870120102

7 January 2021

Somatic mosaicism for partial paternal isodisomy in Wiedemann-Beckwith syndrome: a post-fertilization event

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870120102

7 January 2021

Assignment of anonymous DNA probes to specific intervals of human chromosomes 16 and X.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870120102

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

https://api.crossref.org/works/10.1002%2FGCC.2870120102

7 January 2021

Cloning the complete human adenine phosphoribosyl transferase gene

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870120102

7 January 2021

Molecular sublocalization and characterization of the 11;22 translocation breakpoint in a malignant rhabdoid tumor

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870120102

7 January 2021

Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870120102

7 January 2021

IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870120102

7 January 2021

Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870120102

7 January 2021

Dinculeotide repear polymorphisms at the D16S164, D16S168 and D16S186 loci at 1621-q22.1

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870120102

7 January 2021

Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870120102

7 January 2021

Six dinucleotide repeat polymorphisms on human chromosome 16q12.1-q24.1.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870120102

7 January 2021

Cytogenetics and molecular genetics of Wilms' tumor of childhood

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870120102

7 January 2021

Isolation and characterisation of (AC)n microsatellite genetic markers from human chromosome 16

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870120102

7 January 2021

Dinucleotide repeat polymorphisms at the D16S260, D16S261, D16S265, D16S266, and D16S267 loci.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870120102

7 January 2021

Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870120102

7 January 2021

Molecular characterization of cytogenetic alterations associated with the Beckwith — Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870120102

7 January 2021

Identifiers

DOI

10.1002/GCC.2870120102

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7534105%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

1 reference