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Article

[Chromosome 1q syndrome and hearing loss: an unusual case].

Laryngo- rhino- otologie - 1 Apr 2006

Schwemmle C, Schulze B, Ptok M

Abstract excerpt

INTRODUCTION: The interstitial deletion of chromosome 1q is a disease of rare incidence, which might be hereditary or caused by spontaneous changes within the chromosome respectively. The phenotype in most cases is based on the loss of macrochromosomal material within the long arm of chromosome 1. The characteristics of this syndrome include pre- and postnatal growth retardation, severe psychomotor retardation,...

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Source

Identifiers

PMID: 16646109
DOI: 10.1055/s-2005-870304

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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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[Chromosome 1q syndrome and hearing loss: an unusual case].PMID 16646109Read ↗

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