Beckwith Wiedemann imprinting defect found in leucocyte but not buccal DNA in a child born small for gestational age (Q34463847)

2 August 2017

0 references

Beckwith Wiedemann imprinting defect found in leucocyte but not buccal DNA in a child born small for gestational age (English)

1 reference

2 August 2017

1

Rinki Murphy

1 reference

2 August 2017

Deborah Mackay

2

1 reference

2 August 2017

Ed A Mitchell

series ordinal

3

1 reference

2 August 2017

publication date

1 November 2012

1 reference

2 August 2017

1 reference

2 August 2017

volume

13

1 reference

2 August 2017

page(s)

99

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2350-13-99

2 August 2017

exact match

0 references

cites work

Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3514203

Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3514203

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3514203

ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3514203

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3514203

The vanishing twin: a review

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3514203

Incidence of hypoglycemia in newborn infants classified by birth weight and gestational age

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3514203

Umbilical hernia. A retrospective study

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3514203

Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome

6 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-99

Risk factors for small-for-gestational-age babies: The Auckland Birthweight Collaborative Study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-99

Abnormal methylation at the KvDMR1 imprinting control region in clinically normal children conceived by assisted reproductive technologies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-99

Birth weight is lower for survivors of the vanishing twin syndrome: a case-control study

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-99

Risk of spontaneous abortion in singleton and twin pregnancies after IVF/ICSI.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-99

Epimutation of the TNDM locus and the Beckwith–Wiedemann syndrome centromeric locus in individuals with transient neonatal diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-99

11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations

21 January 2018

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

Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues

1 reference

12 December 2020

Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Wiedemann-Beckwith syndrome in apparently discordant monozygotic twins

1 reference

12 December 2020

Monozygotic twinning and Wiedemann-Beckwith syndrome

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2350-13-99

1 reference

Dimensions Publication ID

2 August 2017

1053619244

0 references

Fatcat ID

release_l4vwv5sdnbavfp4m527jdljtda

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/l4vwv5sdnbavfp4m527jdljtda

24 November 2022

mapped directly with Wikidata item

PMC publication ID

3514203

1 reference

2 August 2017

1 reference