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Article

A report of a child with a deletion (9)(q34.3): a recognisable phenotype?

Journal of medical genetics - 1 Jul 1997

Ayyash H, Mueller R, Maltby E, Horsfield P, Telford N, Tyler R

Abstract excerpt

We report a case of a male infant who presented with congenital anomalies and was found to have a de novo deletion in the terminal region of the long arm of chromosome 9. He died at the age of 17 weeks of cardiorespiratory failure owing to RSV positive bronchiolitis. A review of previously published reports documented one previous report of a patient with a deletion of (9)(q34.3) and multiple congenital...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 9222977
DOI: 10.1136/jmg.34.7.610
PMCID: PMC1051009

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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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