Allelic deletion at 11q23 is common in MYCN single copy neuroblastomas (Q57262605)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10490829%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

title

Allelic deletion at 11q23 is common in MYCN single copy neuroblastomas (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10490829%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10490829%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

author name string

Guo C

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10490829%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

White PS

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10490829%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

Weiss MJ

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10490829%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

Hogarty MD

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10490829%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

Stram DO

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10490829%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

Gerbing R

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10490829%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

Matthay KK

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10490829%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

Seeger RC

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10490829%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

Brodeur GM

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10490829%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

Maris JM

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10490829%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

language of work or name

English

0 references

publication date

1 September 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10490829%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10490829%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

volume

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10490829%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

issue

35

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10490829%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

page(s)

4948-4957

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10490829%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/sj.onc.1202887

31 October 2019

exact match

0 references

cites work

A high-resolution STS, EST, and gene-based physical map of the hereditary paraganglioma region on chromosome 11q23.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

Amplification of N-myc in untreated human neuroblastomas correlates with advanced disease stage

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

Biology and genetics of human neuroblastomas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

Chromosomal aberrations in human neuroblastomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

A proposed staging for children with neuroblastoma.Children's cancer study group A

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

Nonparametric Estimation from Incomplete Observations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

Cloning, chromosomal localization, physical mapping, and genomic characterization of HKR3

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

Genetics of chromosome 11: loci for pediatric and adult malignancies, developmental disorders, and other diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

21 January 2018

Familial neuroblastoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

A Gene Map of the Human Genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

Histopathologic prognostic factors in neuroblastic tumors: definition of subtypes of ganglioneuroblastoma and an age-linked classification of neuroblastomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

An increased NM23H1 copy number may be a poor prognostic factor independent of LOH on 1p in neuroblastomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

Genetic heterogeneity of neuroblastoma studied by comparative genomic hybridization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

Novel regions of chromosomal loss in familial neuroblastoma by comparative genomic hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

7 January 2021

High incidence of constitutional balanced translocations in neuroblastoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

7 January 2021

Comparative genomic hybridization (CGH) analysis of neuroblastomas--an important methodological approach in paediatric tumour pathology

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

7 January 2021

Allelic loss of the short arm of chromosome 4 in neuroblastoma suggests a novel tumour suppressor gene locus

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

7 January 2021

Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

7 January 2021

Regression Models and Life-Tables (with discussion)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

7 January 2021

Representational difference analysis and loss of heterozygosity studies detect 3p deletions in neuroblastoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

7 January 2021

Molecular genetic analysis of familial neuroblastoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

7 January 2021

Prognostic value of immunocytologic detection of bone marrow metastases in neuroblastoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

7 January 2021

Deletion of chromosome 11 and of 14q sequences in neuroblastoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

7 January 2021

Sensitive and reliable detection of genomic imbalances in human neuroblastomas using comparative genomic hybridisation analysis.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1202887

7 January 2021

Identifiers

DOI

10.1038/SJ.ONC.1202887

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10490829%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

1 reference