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Article

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

Clinical genetics - 1 Mar 2012

Eggermann T, Spengler S, Begemann M, Binder G, Buiting K, Albrecht B, Spranger S

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 22211632
DOI: 10.1111/j.1399-0004.2011.01719.x

Genes

MEST

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Deletion of the paternal allele of the imprinted MEST/PEG1 region in a patient with Silver-Russell syndrome features.PMID 22211632Read ↗

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

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