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Article

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

17 Dec 2008

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Share to Epigenetics and DNA Methylation
Share to Genetic Syndromes and Imprinting
Share to Prenatal Screening and Diagnostics

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 19092779
DOI: 10.1038/ejhg.2008.233

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Related research

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Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith–Wiedemann syndromePMID 19092779Read ↗

Lessons from imprinted multilocus loss of methylation in human syndromes: A step toward understanding the mechanisms underlying these complex diseasesSemantic proximity Read ↗

Altered expression of the imprinted transcription factor PLAGL1 deregulates a network of genes in the human IUGR placentaSemantic proximity Read ↗

Beckwith–Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villiSemantic proximity Read ↗

Genome-wide methylation analysis in Silver–Russell syndrome patientsSemantic proximity Read ↗

Loss of CpG Methylation Is Strongly Correlated with Loss of Histone H3 Lysine 9 Methylation at DMR-LIT1 in Patients with Beckwith-Wiedemann SyndromeSemantic proximity Read ↗

Silver-Russell syndrome in a girl born after in vitro fertilization: partial hypermethylation at the differentially methylated region of PEG1/MESTSemantic proximity Read ↗

Maternally inherited autosomal dominant PLAG-1 related Silver Russell syndrome in a fetus with intra-uterine growth restriction.Semantic proximity Read ↗

Paternal Uniparental Disomy of the Entire Chromosome 20 in a Child with Beckwith-Wiedemann Syndrome.Semantic proximity Read ↗

Imprinting at the PLAGL1 domain is contained within a 70-kb CTCF/cohesin-mediated non-allelic chromatin loop.Semantic proximity Read ↗

Genomic Imprinting at the Porcine PLAGL1 Locus and the Orthologous Locus in the Human.Semantic proximity Read ↗

Imprints of disease at GNAS1.Semantic proximity Read ↗

Germline variants in genes of the subcortical maternal complex and Multilocus Imprinting Disturbance are associated with miscarriage/infertility or Beckwith–Wiedemann progenySemantic proximity Read ↗

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