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Article

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

15 Feb 2007

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Share to Assisted Reproductive Technology and Twin Pregnancy
Share to Genetic Syndromes and Imprinting
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 17450433
DOI: 10.1007/s10815-006-9096-3

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Silver-Russell syndrome in a girl born after in vitro fertilization: partial hypermethylation at the differentially methylated region of PEG1/MESTPMID 17450433Read ↗

Deletion of the paternal allele of the imprinted MEST/PEG1 region in a patient with Silver-Russell syndrome features.Semantic proximity Read ↗

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Clinically Distinct Epigenetic Subgroups in Silver-Russell Syndrome: The Degree of H19 Hypomethylation Associates with SRS Phenotype Severity and Genital and Skeletal AnomaliesSemantic proximity Read ↗

Identification of a DNA methylation episignature for recurrent constellations of embryonic malformationsSemantic proximity Read ↗

Discrepant molecular and clinical diagnoses in Beckwith-Wiedemann and Silver-Russell syndromesSemantic proximity Read ↗

Unraveling epigenomic abnormality in azoospermic human males by WGBS, RNA-Seq, and transcriptome profiling analysesSemantic proximity Read ↗

Prenatal Detection of Silver-Russell Syndrome: A First Trimester Suspicion and Diagnostic ApproachSemantic proximity Read ↗

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