(Q73515268)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10704684%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

title

High frequency of loss of heterozygosity for 1p35-p36 (D1S247) in Wilms tumor (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10704684%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

1 reference

R Steinberg

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10704684%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

E Freud

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10704684%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

M Zer

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10704684%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

I Ziperman

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10704684%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Y Goshen

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10704684%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

S Ash

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10704684%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

J Stein

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10704684%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

R Zaizov

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10704684%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

S Avigad

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10704684%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

publication date

1 March 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10704684%20AND%20SRC:MED&resulttype=core&format=json

Cancer Genetics and Cytogenetics

4 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10704684%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

volume

117

1 reference

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4 November 2019

page(s)

136-139

1 reference

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4 November 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10704684%20AND%20SRC:MED&resulttype=core&format=json

ASSOCIATION OF WILMS'S TUMOR WITH ANIRIDIA, HEMIHYPERTROPHY AND OTHER CONGENITAL MALFORMATIONS

4 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2899%2900165-X

7 January 2021

Wilms tumor locus on 11p13 defined by multiple CpG island-associated transcripts

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2899%2900165-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2899%2900165-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2899%2900165-X

7 January 2021

Alternative splicing and genomic structure of the Wilms tumor gene WT1

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2899%2900165-X

7 January 2021

Loss of heterozygosity at 11p13 in Wilms' tumours does not necessarily involve mutations in the WT1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2899%2900165-X

7 January 2021

Infrequent mutation of theWT1 gene in 77 Wilms' tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2899%2900165-X

7 January 2021

WT1 mutations in patients with Denys-Drash syndrome: a novel mutation in exon 8 and paternal allele origin

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2899%2900165-X

7 January 2021

Evidence that WT1 mutations in Denys — Drash syndrome patients may act in a dominant-negative fashion

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2899%2900165-X

7 January 2021

Germline and somatic abnormalities of chromosome 7 in Wilms' tumor

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2899%2900165-X

7 January 2021

Comparative genomic hybridization analysis of Wilms tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2899%2900165-X

7 January 2021

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2899%2900165-X

7 January 2021

PCR assay for chromosome 1p deletion in small neuroblastoma samples

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2899%2900165-X

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/10.1016%2FS0165-4608%2899%2900165-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2899%2900165-X

7 January 2021

Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12–q21

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2899%2900165-X

7 January 2021

Clinicopathologic correlates of loss of heterozygosity in Wilm's tumor: a preliminary analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2899%2900165-X

7 January 2021

Genomic instability in 1p and human malignancies

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2899%2900165-X

7 January 2021

Two distinct deleted regions on the short arm of chromosome I in neuroblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2899%2900165-X

7 January 2021

There may be two tumor suppressor genes on chromosome arm 1p closely associated with biologically distinct subtypes of neuroblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2899%2900165-X

7 January 2021

Prognostic relevance of genetic alterations in the p32 region of chromosome 1 in neuroblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2899%2900165-X

7 January 2021

Monoallelically expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2899%2900165-X

7 January 2021

10.1016/S0165-4608(99)00165-X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10704684%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

1 reference