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Article

Insertion and deletion mutations in the dinucleotide repeat region of the Norrie disease gene in patients with advanced retinopathy of prematurity

1 Apr 2001

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Share to Mitochondrial Function and Pathology
Share to Neonatal Health and Biochemistry
Share to Retinopathy of Prematurity Studies

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 11322656
DOI: 10.1007/s100380170085

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Related research

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Insertion and deletion mutations in the dinucleotide repeat region of the Norrie disease gene in patients with advanced retinopathy of prematurityPMID 11322656Read ↗

Norrie disease gene sequence variants in an ethnically diverse population with retinopathy of prematurity.Semantic proximity Read ↗

Three novel and two recurrent mutations of the Norrie disease gene in patients with Norrie syndrome.Semantic proximity Read ↗

Identification of missense mutations in the Norrie disease gene associated with advanced retinopathy of prematurity.Semantic proximity Read ↗

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Mutations of the Norrie gene in Korean ROP infants.Semantic proximity Read ↗

Mutations in the <i>NDP</i> gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematuritySemantic proximity Read ↗

A mutation in the Norrie disease gene (NDP) associated with familial exudative vitreoretinopathy.Semantic proximity Read ↗

A C597-->A polymorphism in the Norrie disease gene is associated with advanced retinopathy of prematurity in premature Kuwaiti infants.Semantic proximity Read ↗

Two novel mutations in the Norrie disease gene associated with the classical ocular phenotype.Semantic proximity Read ↗

A novel mutation in the Norrie disease gene.Semantic proximity Read ↗

Missense mutations in the NDP gene in patients with a less severe course of Norrie disease.Semantic proximity Read ↗

Planned preterm delivery and treatment of retinal neovascularization in Norrie disease.Semantic proximity Read ↗

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