(Q36740675)

16 August 2017

Cancer risk in patients with constitutional chromosome deletions: a nationwide British cohort study (English)

1 reference

16 August 2017

A J Swerdlow

1

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Minouk J Schoemaker

series ordinal

2

object named as

M J Schoemaker

1 reference

16 August 2017

C D Higgins

3

1 reference

16 August 2017

A F Wright

series ordinal

4

1 reference

16 August 2017

P A Jacobs

series ordinal

5

1 reference

16 August 2017

language of work or name

English

0 references

publication date

27 May 2008

1 reference

British Journal of Cancer

16 August 2017

1 reference

16 August 2017

98

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16 August 2017

12

1 reference

16 August 2017

1929-1933

1 reference

https://scigraph.springernature.com/pub.10.1038/sj.bjc.6604391

16 August 2017

0 references

cites work

The role of chromosomal alterations in human cancer development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2441964

Common fragile sites, extremely large genes, neural development and cancer

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2441964

Allelic loss in human papillomavirus-positive and -negative vulvar squamous cell carcinomas

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2441964

Risk of cancer during the first four years of life in children from The Beckwith-Wiedemann Syndrome Registry

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2441964

A breakpoint map of recurrent chromosomal rearrangements in human neoplasia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2441964

Loss of heterozygosity in cervical carcinoma: subchromosomal localization of a putative tumor-suppressor gene to chromosome 11q22-q24

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2441964

Statistical methods in cancer research. Volume II--The design and analysis of cohort studies

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2441964

Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2441964

Cytogenetic characterization of tumors of the vulva and vagina

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2441964

The 11q terminal deletion disorder: a prospective study of 110 cases.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2441964

Constitutional chromosome aberrations as pathogenetic events in hematologic malignancies.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2441964

The chromosomal basis of human neoplasia.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2441964

Population-based study of cancer among carriers of a constitutional structural chromosomal rearrangement

5 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FSJ.BJC.6604391

Identification of a 6-cM minimal deletion at 11q23.1-23.2 and exclusion of PPP2R1B gene as a deletion target in cervical cancer

21 January 2018

1 reference

12 December 2020

Loss of heterozygosity at 11q23.3 in vasculoinvasive and metastatic squamous cell carcinoma of the cervix

1 reference

12 December 2020

Evaluation of constitutional chromosome aberrations in hematologic disorders

1 reference

12 December 2020

A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities

1 reference

12 December 2020

Frequency of constitutional chromosome alterations in patients with hematologic neoplasias

1 reference

12 December 2020

Recurrent deletions of chromosomes 11q and 3p in anal canal carcinoma

1 reference

12 December 2020

Physical linkage of the fragile site FRA11B and a Jacobsen syndrome chromosome deletion breakpoint in 11q23.3.

1 reference

12 December 2020

Allelic imbalance at chromosome region 11q23 in cervical carcinomas

1 reference

12 December 2020

Identifiers

DOI

10.1038/SJ.BJC.6604391

1 reference

16 August 2017

1 reference

16 August 2017

1 reference