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Article

A small terminal deletion 11q in a boy without Jacobsen syndrome: narrowing the critical region for the 11q Jacobsen syndrome phenotype.

American journal of medical genetics. Part A - 1 Mar 2012

Evers Christina, Janssen Johannes W G, Jauch Anna, Bonin Michael, Moog Ute

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Share to Child, Preschool
Share to Chromosome Banding
Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 11

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

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Identifiers

PMID: 22302716
DOI: 10.1002/ajmg.a.34433

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A small terminal deletion 11q in a boy without Jacobsen syndrome: narrowing the critical region for the 11q Jacobsen syndrome phenotype.PMID 22302716Read ↗

The 11q terminal deletion disorder: a prospective study of 110 cases.Semantic proximity Read ↗

Prenatal diagnosis of a large de novo terminal deletion of chromosome 11q.Semantic proximity Read ↗

Jacobsen syndrome: Advances in our knowledge of phenotype and genotype.Semantic proximity Read ↗

Deletion of 11q24.2-qter in a male child with cleft lip and palate: an atypical feature of Jacobsen syndrome.Semantic proximity Read ↗

Diagnosis and fine mapping of a deletion in distal 11q in two Chinese patients with developmental delay.Semantic proximity Read ↗

A patient with a de novo 11q24.2-->qter deletion.Semantic proximity Read ↗

Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases.Semantic proximity Read ↗

A novel case of bilateral high myopia, cataract, and total retinal detachment associated with interstitial 11q deletion.Semantic proximity Read ↗

A critical region for ulnar defects in patients with 4q deletions may be narrowedSemantic proximity Read ↗

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Partial deletion of the long arm of chromosome 11: ten Japanese children.Semantic proximity Read ↗

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