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Article

De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association

3 Apr 2013

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

Identifiers

PMID: 23549274
DOI: 10.1038/ejhg.2013.58

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL associationPMID 23549274Read ↗

De novo microduplication at 22q11.21 in a patient with VACTERL associationSemantic proximity Read ↗

Phenotypic diversity of patients diagnosed with VACTERL association.Semantic proximity Read ↗

Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations.Semantic proximity Read ↗

Clinical geneticists' views of VACTERL/VATER associationSemantic proximity Read ↗

Evidence for inheritance in patients with VACTERL associationSemantic proximity Read ↗

Exome survey of individuals affected by VATER/VACTERL with renal phenotypes identifies phenocopies and novel candidate genes.Semantic proximity Read ↗

A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL AnomaliesSemantic proximity Read ↗

VACTERL phenotype with mosaic trisomy 5 and uniparental disomy 5.Semantic proximity Read ↗

Underlying genetic factors of the VATER/VACTERL association with special emphasis on the "Renal" phenotype.Semantic proximity Read ↗

Familial occurrence of the VATER/VACTERL association.Semantic proximity Read ↗

[VACTERL-H association with tibial agenesis. Expansion of the clinical phenotype?].Semantic proximity Read ↗

Inheritance of the VATER/VACTERL association.Semantic proximity Read ↗

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