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Article

[3q29 microduplication syndrome].

Anales de pediatria (Barcelona, Spain : 2003) - 1 Dec 2011

Aleixandre Blanquer F, Manchón Trives I, Forniés Arnau M J, Alcaraz Mas L A, Picó Alfonso N, Galán Sánchez F

Abstract excerpt

3q29 microduplication (MIM 611936) is rare syndrome characterized by moderate mental retardation, craniofacial dysmorphic features and musculoskeletal anomalies. The size of the minimal critical region is about 1.73 Mb. It is flanked by repetitive sequences and it is similar in size to the reciprocal 3q29 microdeletion, suggesting a non-allelic homologous recombination event (NAHR) at flanking LCR sequences as...

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Identifiers

PMID: 21982553
DOI: 10.1016/j.anpedi.2011.08.002

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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