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Article

Phenotype and micro-array characterization of duplication 11q22.1-q25 and review of the literature.

Gene - 25 Apr 2013

Ben-Abdallah-Bouhjar Inesse, Mougou-Zerelli Soumya, Hannachi Hanene, Ben-Khelifa Hela, Soyah Najla, Labalme Audrey, Sanlaville Damien, Elghezal Hatem, Saad Ali

Abstract excerpt

Partial duplication of 11q is related to several malformations like growth retardation, intellectual disability, hypoplasia of corpus callosum, short nose, palate defects, cardiac, urinary tract abnormalities and neural tube defects. We have studied the clinical and molecular characteristics of a...

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Share to Abnormalities, Multiple
Share to Chromosomes, Human, Pair 11
Share to Chromosomes, Human, Pair 7

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Comparative Genomic Hybridization

Share to Karyotyping

Share to Microarray Analysis

Share to Translocation, Genetic

Share to Trisomy

Source

Identifiers

PMID: 23403231
DOI: 10.1016/j.gene.2013.01.017

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23403231-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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