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Article

A Fryns syndrome-like phenotype with mosaic t(1;22)(q12;p12) chromosomal translocation.

Clinical dysmorphology - 1 Apr 2004

Ahmed Atif A, Gilbert-Barness Enid

Abstract excerpt

We report a case of Fryns syndrome-like phenotype with chromosomal translocation. Not all such cases have chromosomal abnormalities hence we suggest that this condition is associated with genetic heterogeneity and variable clinical manifestations.

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Source

Identifiers

PMID: 15057129

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15057129-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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