Fetal growth patterns in Beckwith-Wiedemann syndrome. (Q40013334)

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7 March 2020

title

Fetal growth patterns in Beckwith-Wiedemann syndrome (English)

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7 March 2020

1

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Donatella Milani

13

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Andrea Riccio

20

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Giovanni Battista Ferrero

7 March 2020

21

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author name string

S Russo

2

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7 March 2020

A de Crescenzo

3

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A Freschi

4

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7 March 2020

L Calzari

5

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S Maitz

6

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M Macchiaiolo

7

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C Molinatto

8

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G Baldassarre

9

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M Mariani

10

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L Tarani

11

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M F Bedeschi

12

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D Melis

14

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7 March 2020

A Bartuli

15

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M V Cubellis

16

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A Selicorni

17

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M C Silengo

18

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L Larizza

19

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publication date

15 March 2016

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7 March 2020

number of pages

7

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based on heuristic

inferred from page(s)

published in

Clinical Genetics

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volume

90

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issue

1

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page(s)

21-27

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Clinical utility gene card for: Beckwith-Wiedemann Syndrome.

7 March 2020

cites work

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Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.

21 January 2018

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Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor

21 January 2018

1 reference

Molecular findings in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases

21 January 2018

1 reference

Maternal gametic transmission of translocations or inversions of human chromosome 11p15.5 results in regional DNA hypermethylation and downregulation of CDKN1C expression

21 January 2018

1 reference

An 11p15 imprinting centre region 2 deletion in a family with Beckwith Wiedemann syndrome provides insights into imprinting control at CDKN1C.

21 January 2018

1 reference

A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome.

21 January 2018

1 reference

(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

Beckwith-Wiedemann syndrome: growth pattern and tumor risk according to molecular mechanism, and guidelines for tumor surveillance

21 January 2018

1 reference

Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjects

21 January 2018

1 reference

Nephrological findings and genotype-phenotype correlation in Beckwith-Wiedemann syndrome.

21 January 2018

1 reference

Tumor risk in Beckwith-Wiedemann syndrome: A review and meta-analysis.

21 January 2018

1 reference

Screening for Wilms tumor in children with Beckwith-Wiedemann syndrome or idiopathic hemihypertrophy

21 January 2018

1 reference

Screening Hepatoblastoma in Beckwith-Wiedemann Syndrome: A Complex Issue.

21 January 2018

1 reference

(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome: a paradigm for genomic medicine.

21 January 2018

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Determination of KCNQ1OT1 and H19 methylation levels in BWS and SRS patients using methylation-sensitive high-resolution melting analysis

21 January 2018

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Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome.

21 January 2018

1 reference

A fluorescent method for detecting low-grade 11patUPD mosaicism in Beckwith–Wiedemann syndrome

21 January 2018

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Significance of neonatal body indices in identifying fetal macrosomia

21 January 2018

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Use of anthropometric indices to reveal nutritional status: normative data from 10,226 Chinese neonates

21 January 2018

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Novel fetal and maternal sonographic findings in confirmed cases of Beckwith-Wiedemann syndrome

21 January 2018

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Relevance of genomic imprinting in intrauterine human growth expression of CDKN1C, H19, IGF2, KCNQ1 and PHLDA2 imprinted genes

21 January 2018

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Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome.

21 January 2018

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Insulin-like growth factor II (IGF-II) and the IGF-II/mannose-6-phosphate receptor: the myth continues

21 January 2018

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Developmental adaptations to increased fetal nutrient demand in mouse genetic models of Igf2-mediated overgrowth.

21 January 2018

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

21 January 2018

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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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Fetal overgrowth in the Cdkn1c mouse model of Beckwith-Wiedemann syndrome

21 January 2018

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CDKN1C mutations in HELLP/preeclamptic mothers of Beckwith-Wiedemann Syndrome (BWS) patients.

21 January 2018

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Deficiency in p57Kip2 expression induces preeclampsia-like symptoms in mice

21 January 2018

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

21 January 2018

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Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome

21 January 2018

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21 January 2018

Identifiers

DOI

10.1111/CGE.12759

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26857110%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

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