Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. (Q35248407)

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1 October 2019

title

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15 (English)

1 reference

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Beckwith-Wiedemann syndrome

1 October 2019

main subject

1 reference

5

M Boehnke

1 reference

PubMed publication ID

7 August 2017

A J Ping

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2565083%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

A E Reeve

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2565083%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

D J Law

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2565083%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

M R Young

4

1 reference

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1 October 2019

A P Feinberg

6

1 reference

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1 October 2019

M Boehnke

5

1 reference

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1 October 2019

language of work or name

English

0 references

publication date

1 May 1989

1 reference

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American Journal of Human Genetics

1 October 2019

published in

1 reference

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1 October 2019

volume

44

1 reference

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1 October 2019

issue

5

1 reference

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1 October 2019

page(s)

720-723

1 reference

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Sequential tests for the detection of linkage

1 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715646

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715646

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715646

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715646

Polymorphic DNA region adjacent to the 5' end of the human insulin gene

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715646

A locus on chromosome 11p with multiple restriction site polymorphisms

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715646

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715646

A genetic linkage map of the human genome.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715646

Wilms' tumor, overgrowth, and fetal growth factors: a hypothesis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715646

27 July 2018

Genetics of human cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715646

Age distribution of Wilms' tumor: report from the National Wilms' Tumor Study.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715646

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715646

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715646

Incidence of childhood cancer: experience of a decade in a population-based registry.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715646

Deletion of chromosome 11(p11p13) in a patient with Beckwith-Wiedemann syndrome

26 September 2018

1 reference

12 December 2020

Wiedemann-Beckwith syndrome in apparently discordant monozygotic twins

1 reference

12 December 2020

Programs for pedigree analysis: Mendel, Fisher, and dGene

1 reference

12 December 2020

Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism

1 reference

12 December 2020

Chromosome 11 and Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Identifiers

1 reference

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1 October 2019

PubMed publication ID

2565083

1 reference