(Q43145512)

14 November 2017

Genomic imprinting and the Beckwith-Wiedemann syndrome (English)

1 reference

14 November 2017

Brown KW

1

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14 November 2017

Williams JC

series ordinal

2

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14 November 2017

Maitland NJ

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3

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14 November 2017

Mott MG

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4

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14 November 2017

language of work or name

English

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publication date

1 May 1990

1 reference

American Journal of Human Genetics

14 November 2017

1 reference

14 November 2017

46

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14 November 2017

1000-1001

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14 November 2017

5

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

14 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683593

Genomic imprinting and carcinogenesis

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683593

Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683593

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683593

Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683593

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683593

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683593

Trisomy 11p15 and Beckwith-Wiedemann syndrome. Report of two new cases

15 August 2018

1 reference

12 December 2020

Bronze baby syndrome, biliary hypoplasia, incomplete Beckwith-Wiedemann syndrome and partial trisomy 11

1 reference

12 December 2020

Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours

1 reference

12 December 2020

Maternal allele loss in Wilms' tumour

1 reference

12 December 2020

Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma

1 reference

12 December 2020

Identifiers

1 reference

14 November 2017

1 reference