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Article

Ring chromosome 13 in an Omani infant boy with mental retardation and multiple congenital anomalies.

Saudi medical journal - 1 Sept 2001

Venugopalan P, Kenue R K

Abstract excerpt

An Omani infant boy with severe physical and psychomotor retardation, facial dysmorphism, and anomalies of the cardiovascular and genito-urinary systems is described. The chromosomal analysis revealed a 46, XY, r (13) (p11;q34) karyotype. The cytogenetic basis of this rare abnormality is outlined and phenotypic features are compared with published reports.

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Share to Chromosomes, Human, Pair 13
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 11590457

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Ring chromosome 13 in an Omani infant boy with mental retardation and multiple congenital anomalies.PMID 11590457Read ↗

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