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Article

Classic Rett syndrome in a boy as a result of somatic mosaicism for a MECP2 mutation.

Annals of neurology - 1 Nov 2001

Armstrong J, Pineda M, Aibar E, Geán E, Monrós E

Abstract excerpt

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Topics

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Share to Chromosomal Proteins, Non-Histone
Share to In Situ Hybridization, Fluorescence
Share to Karyotyping
Share to Klinefelter Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Methyl-CpG-Binding Protein 2

Share to Mosaicism

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Share to X Chromosome

Source

Identifiers

PMID: 11706982
DOI: 10.1002/ana.1272

Genes

MECP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

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Classic Rett syndrome in a boy as a result of somatic mosaicism for a MECP2 mutation.PMID 11706982Read ↗

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Rett Syndrome: A Timely Review From Recognition to Current Clinical Approaches and Clinical Study Updates.Semantic proximity Read ↗

Novel clinical finding in MECP2 duplication syndrome.Semantic proximity Read ↗

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Mutation analysis in the MECP2 gene and genetic counselling for Rett syndrome.Semantic proximity Read ↗

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