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Article

In Vitro Fertilization May Increase the Risk of Beckwith-Wiedemann Syndrome Related to the Abnormal Imprinting of the KCNQ1OT Gene

23 Apr 2003

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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 About Contact Helena Bioinformatics

Identifiers

PMID: 12772698
DOI: 10.1086/374824

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Related research

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Research trail→

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In Vitro Fertilization May Increase the Risk of Beckwith-Wiedemann Syndrome Related to the Abnormal Imprinting of the KCNQ1OT GenePMID 12772698Read ↗

The 5' end of the KCNQ1OT1 gene is hypomethylated in the Beckwith-Wiedemann syndrome.Semantic proximity Read ↗

Beckwith-Wiedemann Syndrome: Historical, Clinicopathological, and Etiopathogenetic PerspectivesSemantic proximity Read ↗

Clinical and molecular analyses of Beckwith-Wiedemann syndrome: Comparison between spontaneous conception and assisted reproduction techniques.Semantic proximity Read ↗

Beckwith-Wiedemann Syndrome and IVF: A Case-Control StudySemantic proximity Read ↗

Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann SyndromeSemantic proximity Read ↗

Beckwith-Wiedemann syndrome and assisted reproduction technology (ART): Table 1Semantic 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 ↗

First report of a successful pregnancy by preimplantation genetic testing for Beckwith-Wiedemann syndrome.Semantic proximity Read ↗

The epigenetic imprinting defect of patients with Beckwith—Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 regionSemantic proximity Read ↗

Imprinting disruption of the <i>CDKN1C</i>/<i>KCNQ1OT1</i> domain: the molecular mechanisms causing Beckwith-Wiedemann syndrome and cancerSemantic proximity Read ↗

Novel deleterious splicing variant in HFM1 causes gametogenesis defect and recurrent implantation failure: concerning the risk of chromosomal abnormalities in embryosSemantic proximity Read ↗

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangementsSemantic proximity Read ↗

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