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Article

Clinical aspects of the fragile X syndrome.

Results and problems in cell differentiation - 1 Jan 2012

Brown W Ted

Abstract excerpt

Fragile X syndrome patients express a wide array of cognitive and other gender-specific phenotypic features. These manifestations result not only from molecular mechanisms that are altered as a result of the expansion of a CGG-repeat region in the FMR1 promoter, but also genetic factors such as founder effects and mosaicism. In this chapter, I will summarize the many and varied features of fragile X syndrome as...

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Source

Identifiers

PMID: 22009358
DOI: 10.1007/978-3-642-21649-7_15

Genes

FMR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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