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Article

Duane's syndrome and 22 marker chromosome: a possible cat-eye syndrome.

Acta paediatrica (Oslo, Norway : 1992) - 1 Nov 2006

Gómez-Lado Carmen, Eirís Jesús, Martínez-Yriarte José Manuel, Blanco Oscar, Castro-Gago Manuel

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Share to Abnormalities, Multiple
Share to Child, Preschool
Share to Chromosomes, Human, Pair 22
Share to Ear, External

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Markers

Share to Heart Septal Defects, Atrial

Share to In Situ Hybridization, Fluorescence

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Identifiers

PMID: 17062489
DOI: 10.1080/08035250600622826

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Duane's syndrome and 22 marker chromosome: a possible cat-eye syndrome.PMID 17062489Read ↗

Confirmation of linkage of Duane's syndrome and refinement of the disease locus to an 8.8-cM interval on chromosome 2q31Semantic proximity Read ↗

Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrome.Semantic proximity Read ↗

Partial trisomy of chromosome 22 resulting from an interstitial duplication of 22q11.2 in a child with typical cat eye syndrome.Semantic proximity Read ↗

Wide clinical variability in cat eye syndrome patients: four non-related patients and three patients from the same family.Semantic proximity Read ↗

Maternal derivation of inv dup (22) and clinical variation in cat-eye syndrome.Semantic proximity Read ↗

Partial tetrasomy of chromosome 22q11.1 resulting from a supernumerary isodicentric marker chromosome in a boy with cat-eye syndrome.Semantic proximity Read ↗

Cat eye syndrome: Clinical, cytogenetics and familial findings in a large cohort of 43 patients highlighting the importance of congenital heart disease and inherited casesSemantic proximity Read ↗

Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.Semantic proximity Read ↗

Cat eye syndrome and growth hormone deficiency with pituitary anomalies: a case report and review of the literature.Semantic proximity Read ↗

A new case of a severe clinical phenotype of the cat-eye syndrome.Semantic proximity Read ↗

Growth hormone deficiency and pituitary malformation in a recurrent Cat-Eye syndrome: A family reportSemantic proximity Read ↗

Phenotypic expansion of the supernumerary derivative (22) chromosome syndrome: VACTERL and Hirschsprung's disease.Semantic proximity Read ↗

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