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Article

[A case report of genetic analysis in the OCRL1 gene in Lowe syndrome].

Zhonghua er ke za zhi = Chinese journal of pediatrics - 1 Sept 2012

Jiang Fang, Gao Yan, Ou Zhi-ying

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PMID: 23158824

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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[A case report of genetic analysis in the OCRL1 gene in Lowe syndrome].PMID 23158824Read ↗

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[Analysis of OCRL gene variant in a Chinese pedigree affected with Lowe syndrome].Semantic proximity Read ↗

Novel mutation of OCRL1 in Lowe syndrome with multiple epidermal cysts.Semantic proximity Read ↗

Novel mutation of OCRL1 in Lowe syndrome.Semantic proximity Read ↗

Two cases of Lowe syndrome caused by a novel mutation in OCRL gene in a familySemantic proximity Read ↗

[Clinical and genetic analysis of an infant with Lowe syndrome caused by exonic duplication of OCRL gene].Semantic proximity Read ↗

Physical mapping and genomic structure of the Lowe syndrome gene OCRL1Semantic proximity Read ↗

OCRL mutation analysis in Italian patients with Lowe syndrome.Semantic proximity Read ↗

Novel OCRL1 gene mutations in six Chinese families with Lowe syndrome.Semantic proximity Read ↗

Prenatal diagnosis of lowe syndrome: identification of a novel pathogenic variation in the OCRL1gene.Semantic proximity Read ↗

Genotype-Phenotype Correlation Reanalysis in 83 Chinese Cases with OCRL Mutations.Semantic proximity Read ↗

[Clinical and genetic results with reference to corneal alterations in Lowe-syndrome].Semantic proximity Read ↗

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