(Q37478188)

20 August 2017

Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome (English)

1 reference

20 August 2017

0 references

1 reference

Mariarosaria Calvello

Mariarosaria Calvello

1

0 references

Silvia Tabano

Silvia Tabano

2

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Silvia Sirchia

Silvia M Sirchia

15

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Daniela Perotti

Daniela Perotti

11

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Monica Miozzo

Monica Miozzo

16

0 references

Filippo Spreafico

Filippo Spreafico

9

0 references

Lidia Larizza

12

Lidia Larizza

1 reference

20 August 2017

Patrizia Colapietro

3

1 reference

20 August 2017

Silvia Maitz

4

1 reference

20 August 2017

Alessandra Pansa

5

1 reference

20 August 2017

Claudia Augello

6

1 reference

20 August 2017

Faustina Lalatta

7

1 reference

20 August 2017

Barbara Gentilin

8

1 reference

20 August 2017

Luciano Calzari

10

1 reference

20 August 2017

Silvia Russo

13

1 reference

20 August 2017

Angelo Selicorni

14

1 reference

20 August 2017

5 August 2013

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20 August 2017

1 reference

20 August 2017

8

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20 August 2017

10

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20 August 2017

1053-1060

1 reference

Prognostic value of three different methods of MGMT promoter methylation analysis in a prospective trial on newly diagnosed glioblastoma

20 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3891686

Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3891686

Sensitive and quantitative universal Pyrosequencing methylation analysis of CpG sites

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3891686

Uniparental paternal disomy in a genetic cancer-predisposing syndrome

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3891686

Molecular findings in Beckwith-Wiedemann syndrome

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3891686

Epigenetic and genetic disturbance of the imprinted 11p15 region in Beckwith-Wiedemann and Silver-Russell syndromes.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3891686

Beckwith-Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3891686

Bilateral pheochromocytomas, hemihyperplasia, and subtle somatic mosaicism: the importance of detecting low-level uniparental disomy.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3891686

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

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3891686

Omphalocele: comparison of outcome following prenatal or postnatal diagnosis

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3891686

Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3891686

Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3891686

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

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3891686

Decreased Placental Methylation at the H19/IGF2 Imprinting Control Region is Associated with Normotensive Intrauterine Growth Restriction but not Preeclampsia

2 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.4161%2FEPI.25812

Seven cases of Wiedmann-Beckwith syndrome, including the first reported case of mosaic paternal isodisomy along the whole chromosome 11

21 January 2018

1 reference

12 December 2020

Prenatal diagnosis of Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Serial pyrosequencing for quantitative DNA methylation analysis

1 reference

12 December 2020

Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Beckwith–Wiedemann syndrome

1 reference

12 December 2020

The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disorders

1 reference

12 December 2020

Identifiers

DOI

10.4161/EPI.25812

1 reference

20 August 2017

1 reference

20 August 2017

PubMed publication ID

23917791

1 reference