(Q52133092)

English

Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome.

scientific article published in June 2001

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/11436121

Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome. (English)

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/11436121

author name string

Gaston V

1

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/11436121

Le Bouc Y

2

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/11436121

Soupre V

3

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/11436121

Burglen L

4

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/11436121

Donadieu J

5

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/11436121

Oro H

6

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/11436121

Audry G

7

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/11436121

Vazquez MP

8

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/11436121

Gicquel C

9

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/11436121

publication date

1 June 2001

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/11436121

European Journal of Human Genetics

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/11436121

9

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/11436121

6

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/11436121

409-418

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/11436121

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular genetics of Wiedemann-Beckwith syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Somatic overgrowth associated with overexpression of insulin-like growth factor II.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

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Isolated hemihyperplasia (hemihypertrophy): Report of a prospective multicenter study of the incidence of neoplasia and review

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Insulin-like growth factor 2 and overgrowth: molecular biology and clinical implications

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Beckwith-Wiedemann syndrome: imprinting in clusters revisited

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

The Beckwith-Wiedemann syndrome phenotype and the risk of cancer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Nephromegaly in infancy and early childhood: a risk factor for Wilms tumor in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Somatic mosaicism for partial paternal isodisomy in Wiedemann-Beckwith syndrome: a post-fertilization event

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

The product of the H19 gene may function as an RNA

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Proportion of cells with paternal 11p15 uniparental disomy correlates with organ enlargement in Wiedemann-beckwith syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Monozygotic twinning and Wiedemann-Beckwith syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Monozygotic twinning and Wiedemann-Beckwith syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Two pairs of male monozygotic twins discordant for Wiedemann-Beckwith syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Non-random X chromosome inactivation in an affected twin in a monozygotic twin pair discordant for Wiedemann-Beckwith syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Epigenetic gene silencing in cancer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Assessment of p57(KIP2) gene mutation in Beckwith-Wiedemann syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200649

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.EJHG.5200649

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/11436121

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/11436121

ResearchGate publication ID

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