Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Eye signs in a child with ROBO3 gene mutation.

Indian journal of ophthalmology - 1 Jul 2022

Yoganathan Sangeetha, Kumar Madhan, Malhotra Mukul, Joy Praisy, Danda Sumita, Thomas Maya, David Kenny S, Jasper Anitha, Selvin Satheesh Solomon T

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Child
Share to Family
Share to Mutation
Share to Receptors, Cell Surface

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Open in PubMed Open full text

Identifiers

PMID: 35791185
DOI: 10.4103/ijo.IJO_2065_21
PMCID: PMC9426051

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Eye signs in a child with ROBO3 gene mutation.PMID 35791185Read ↗

Horizontal Gaze Palsy in Two Brothers with Compound Heterozygous ROBO3 Gene Mutations.Semantic proximity Read ↗

A novel mutation of ROBO3 in horizontal gaze palsy with progressive scoliosis.Semantic proximity Read ↗

CLINICAL EVALUATION OF GENETIC DISEASES OF THE EYE.Semantic proximity Read ↗

A review of the genetics and clinical manifestations of Donnai-Barrow syndrome.Semantic proximity Read ↗

Ocular presentation of Walker-Warburg syndrome with POM2 mutation.Semantic proximity Read ↗

A case of de Barsy syndrome with a severe eye phenotype.Semantic proximity Read ↗

FOXE3 mutations: genotype-phenotype correlations.Semantic proximity Read ↗

Ocular Manifestations in Pediatric Tumor Suppressor Gene Mutations: A Case-Based and Literature Review on RB1, NF1, NF2, VHL, and TSCSemantic proximity Read ↗

Horizontal gaze palsy and progressive scoliosis-a tale of two siblings with ROBO3 mutation.Semantic proximity Read ↗

Horizontal gaze palsy with progressive scoliosis: three novel ROBO3 mutations and descriptions of the phenotypes of four patients.Semantic proximity Read ↗

[The genetic background for the eye malformations anophthalmia and microphthalmia].Semantic proximity Read ↗

Extending the ophthalmological phenotype of Galloway-Mowat syndrome with distinct retinal dysfunction: a report and review of ocular findings.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.