Wiedemann-Beckwith syndrome: further prenatal characterization of the condition (Q34504509)

2 August 2017

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title

Wiedemann-Beckwith syndrome: further prenatal characterization of the condition (English)

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2 August 2017

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Orit Reish

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2 August 2017

Israela Lerer

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2 August 2017

Aliza Amiel

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2 August 2017

Eli Heyman

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2 August 2017

Arie Herman

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2 August 2017

Tzipora Dolfin

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2 August 2017

Dvorah Abeliovich

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2 August 2017

publication date

1 January 2002

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American Journal of Medical Genetics Part A

2 August 2017

published in

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2 August 2017

volume

107

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2 August 2017

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2 August 2017

page(s)

209-213

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Analysis of CDKN1C in Beckwith Wiedemann syndrome.

2 August 2017

cites work

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https://api.crossref.org/works/10.1002%2FAJMG.10143

Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10143

Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10143

Clinical features and natural history of Beckwith-Wiedemann syndrome: presentation of 74 new cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10143

Wiedemann-Beckwith syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10143

Prenatal diagnosis and perinatal management of the Beckwith-Wiedeman syndrome: a case and review

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10143

Chromosome 6q deletions: a report of two additional cases and a review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10143

Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10143

Relaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10143

The sins of the fathers and mothers: genomic imprinting in mammalian development

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10143

Prenatal diagnosis of Wiedemann-Beckwith syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10143

21 January 2018

Identifiers

DOI

10.1002/AJMG.10143

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2 August 2017

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