(Q24308083)

English

Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway

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title

Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway (English)

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main subject

Insulin like growth factor 2

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stated in

GOA release 2020-03-11

regulation of gene expression by genetic imprinting

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stated in

GOA release 2020-03-11

Beckwith-Wiedemann syndrome

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7

W Reik

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author name string

K W Brown

series ordinal

1

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A J Villar

series ordinal

2

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W Bickmore

series ordinal

3

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J Clayton-Smith

series ordinal

4

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D Catchpoole

series ordinal

5

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E R Maher

series ordinal

6

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language of work or name

English

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publication date

December 1996

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published in

Human Molecular Genetics

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volume

5

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page(s)

2027-32

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issue

12

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Identifiers

DOI

10.1093/HMG/5.12.2027

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stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3658328

OpenCitations bibliographic resource ID

3658328

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3658328

PubMed ID

8968759

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(Q24308083)

Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway

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