(Q71668047)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529555%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

title

Localization of Beckwith-Wiedemann and rhabdoid tumor chromosome rearrangements to a defined interval in chromosome band 11p15.5. (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529555%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

1 reference

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529555%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

author name string

Sait SN

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529555%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

Nowak NJ

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529555%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

Singh-Kahlon P

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529555%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

Weksberg R

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529555%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

Shows TB

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529555%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

Higgins MJ

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529555%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

publication date

1 October 1994

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529555%20AND%20SRC:MED&resulttype=core&format=json

Genes, Chromosomes and Cancer

20 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529555%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

volume

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529555%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529555%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

page(s)

97-105

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529555%20AND%20SRC:MED&resulttype=core&format=json

Histopathology and prognosis of Wilms tumorResults from the first national wilms' tumor study

20 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

Molecular analysis of a partial deletion of 22q in a central nervous system rhabdoid tumor

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

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.2870110206

7 January 2021

Malignant rhabdoid tumor: a highly malignant childhood tumor with minimal karyotypic changes.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

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.2870110206

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

Parental genomic imprinting of the human IGF2 gene

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

Tumour-suppressor activity of H19 RNA

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

Molecular detection of chromosomal translocations that disrupt the putative retinoblastoma susceptibility locus

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

Construction of the physical map for three loci in chromosome band 13q14: comparison to the genetic map.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

Imprinting and Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

Establishment of a rhabdoid tumor cell line with a specific chromosomal abnormality, 46,XY,t(11;22)(p15.5;q11.23)

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridization

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

Prognostic relevance of DNA content in childhood renal tumours

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

Fluorescence in situ hybridization of YAC clones after Alu-PCR amplification

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

Human chromosome 11 contains two different growth suppressor genes for embryonal rhabdomyosarcoma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

Cloning of cDNAs of the MLL gene that detect DNA rearrangements and altered RNA transcripts in human leukemic cells with 11q23 translocations

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

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.2870110206

7 January 2021

Recurrent Wiedemann-Beckwith syndrome with inversion of chromosome (11)(p11.2p15.5)

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

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.2870110206

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.2870110206

7 January 2021

11p15.5-specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesis.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

Relaxation of imprinted genes in human cancer.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

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.2870110206

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.2870110206

7 January 2021

Fetal rhabdomyomatous nephroblastoma—A variant of Wilms' tumor

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

Monoallelic expression of the human H19 gene

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870110206

7 January 2021

Identifiers

DOI

10.1002/GCC.2870110206

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529555%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

1 reference