(Q34328129)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19513094%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19513094%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

1

1 reference

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30 January 2020

Roelof-Jan Oostra

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19513094%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

Deborah Jg Mackay

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19513094%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

author name string

Marielle Alders

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19513094%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

Saskia M Maas

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19513094%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

Karin van der Lip

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19513094%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

Johnatan L Callaway

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19513094%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

Alice Brooks

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19513094%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

Sandra van 't Padje

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19513094%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

Andries Westerveld

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19513094%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

Nico J Leschot

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19513094%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

Marcel M A M Mannens

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19513094%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

publication date

10 June 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19513094%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Human Genetics

30 January 2020

published in

1 reference

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30 January 2020

volume

17

1 reference

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30 January 2020

issue

12

1 reference

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30 January 2020

page(s)

1625-1634

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19513094%20AND%20SRC:MED&resulttype=core&format=json

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

30 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987023

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987023

Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987023

Twin-specific intrauterine 'growth' charts based on cross-sectional birthweight data

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987023

The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987023

Imprinting errors and developmental asymmetry

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987023

FAMILIAL MALFORMATION COMPLEX WITH UMBILICAL HERNIA AND MACROGLOSSIA--A "NEW 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=2987023

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987023

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987023

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=2987023

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987023

Imprinting in clusters: lessons from 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=2987023

Twinning: mechanisms and genetic implications

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987023

Some causes of genotypic and phenotypic discordance in monozygotic twin pairs

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987023

Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987023

Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987023

Monozygotic twins discordant for Goldenhar syndrome.

6 July 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.77

Postzygotic mutation and germline mosaicism in the otopalatodigital syndrome spectrum disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.77

Lesch-Nyhan disease in a female with a clinically normal monozygotic twin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.77

New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.77

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.77

Somatic mosaicism for maternal uniparental disomy 15 in a girl with Prader-Willi syndrome: confirmation by cell cloning and identification of candidate downstream genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.77

Monozygotic twins with discordant karyotypes: a case report.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.77

Cell tracing shows the contribution of the yolk sac to adult haematopoiesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.77

Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.77

Sex ratio and placentation in twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.77

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/10.1038%2FEJHG.2009.77

Non-random X chromosome inactivation in an affected twin in a monozygotic twin pair discordant for Wiedemann-Beckwith syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.77

Stem cells: Blood lines from embryo to adult

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.77

Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS

21 January 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Mosaic trisomy 11p in monozygotic twins with discordant clinical phenotypes

1 reference

12 December 2020

Growth of heterokaryotic monozygotic twins discordant for Ullrich-Turner syndrome during the first years of life

1 reference

12 December 2020

Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential

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

1 reference

12 December 2020

Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Number of yolk sacs does not predict amnionicity in early first-trimester monochorionic multiple gestations

1 reference

12 December 2020

Confined blood chimerism in monochorionic dizygous (MCDZ) twins

1 reference

12 December 2020

Imprinting status of 11p15 genes in Beckwith-Wiedemann syndrome patients with CDKN1C mutations

1 reference

12 December 2020

Identifiers

DOI

10.1038/EJHG.2009.77

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19513094%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19513094%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

PubMed publication ID

19513094

1 reference