(Q45234391)

11 December 2017

title

Different methylation patterns in BWS/SRS cases clarified by MS-MLPA. (English)

1 reference

11 December 2017

Mihaela Lukova

1

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11 December 2017

Albena Todorova

series ordinal

2

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11 December 2017

Tihomir Todorov

series ordinal

3

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11 December 2017

Vanyo Mitev

series ordinal

4

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11 December 2017

publication date

20 October 2012

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Molecular Biology Reports

11 December 2017

published in

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11 December 2017

volume

40

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11 December 2017

issue

1

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11 December 2017

page(s)

263-268

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https://scigraph.springernature.com/pub.10.1007/s11033-012-2057-2

11 December 2017

exact match

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-2057-2

Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-2057-2

Silver-Russell syndrome: genetic basis and molecular genetic testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-2057-2

Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-2057-2

Beckwith-Wiedemann syndrome and uniparental disomy 11p: fine mapping of the recombination breakpoints and evaluation of several techniques

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-2057-2

Is maternal duplication of 11p15 associated with Silver-Russell syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-2057-2

Constitutional mosaic genome-wide uniparental disomy due to diploidisation: an unusual cancer-predisposing mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-2057-2

Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development

21 January 2018

1 reference

12 December 2020

Prenatal diagnosis of Beckwith-Wiedemann syndrome

1 reference

12 December 2020

MS-MLPA is a specific and sensitive technique for detecting all chromosome 11p15.5 imprinting defects of BWS and SRS in a single-tube experiment

1 reference

12 December 2020

Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci

1 reference

12 December 2020

Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Use of multiplex ligation-dependent probe amplification increases the detection rate for 11p15 epigenetic alterations in Silver-Russell syndrome

1 reference

12 December 2020

Japanese and North American/European patients with Beckwith-Wiedemann syndrome have different frequencies of some epigenetic and genetic alterations

1 reference

12 December 2020

10.1007/S11033-012-2057-2

Identifiers

DOI

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Dimensions Publication ID

11 December 2017

1016210900

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1 reference