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Article

Molecular cytogenetic and clinical characterization of a patient with a 5.6-Mb deletion in 7p15 including HOXA cluster.

American journal of medical genetics. Part A - 1 Mar 2011

Jun Kyung Ran, Seo Eul-Ju, Lee Jin-Ok, Yoo Han-Wook, Park In-Sook, Yoon Hye-Kyung

Abstract excerpt

Here, we describe the clinical features of a boy with a 5.6-Mb deletion at chromosome 7p15.1-p15.3. He has mild facial anomalies, hand-foot abnormalities, hypospadias, congenital heart defects, and supernumerary nipples. This deletion was detected by array comparative genomic hybridization and verified by fluorescence in situ hybridization using BACs selected from the USCS genome browser. This deletion was not...

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Source

Identifiers

PMID: 21344639
DOI: 10.1002/ajmg.a.33860

Genes

HOXA13
HOXA3

Provenance

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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