(Q51812674)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16575195%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

title

New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndrome (English)

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18 January 2020

1

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18 January 2020

author name string

Rubin T

2

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18 January 2020

Shuman C

3

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18 January 2020

Estabrooks L

4

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18 January 2020

Aylsworth AS

5

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18 January 2020

McDonald MT

6

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18 January 2020

Steele L

7

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18 January 2020

Ray PN

8

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18 January 2020

Weksberg R

9

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18 January 2020

publication date

1 January 2006

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Cytogenetics and Genome Research

18 January 2020

published in

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18 January 2020

volume

113

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18 January 2020

issue

1-4

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18 January 2020

page(s)

313-317

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

18 January 2020

cites work

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Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndrome

21 January 2018

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Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene.

21 January 2018

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Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.

21 January 2018

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21 January 2018

Identifiers

DOI

10.1159/000090847

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16575195%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

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