Found: 15
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Danish heritable retinoblastoma survivors' perspectives on reproductive choices: "It's important for me, not to pass on this condition".
- Published in:
- Journal of Genetic Counseling, 2023, v. 32, n. 1, p. 31, doi. 10.1002/jgc4.1618
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- Publication type:
- Article
Diagnostic yield of candidate genes in an Australian corneal dystrophy cohort.
- Published in:
- Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 10, p. 1, doi. 10.1002/mgg3.2023
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- Publication type:
- Article
Heritability of Strabismus: Genetic Influence Is Specific to Eso-Deviation and Independent of Refractive Error.
- Published in:
- Twin Research & Human Genetics, 2012, v. 15, n. 5, p. 624, doi. 10.1017/thg.2012.22
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- Publication type:
- Article
Mutations in the <i>EPHA2</i> Gene Are a Major Contributor to Inherited Cataracts in South-Eastern Australia.
- Published in:
- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0072518
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- Publication type:
- Article
Mitochondrial Oxidative Phosphorylation Compensation May Preserve Vision in Patients with OPA1-Linked Autosomal Dominant Optic Atrophy.
- Published in:
- PLoS ONE, 2011, v. 6, n. 6, p. 1, doi. 10.1371/journal.pone.0021347
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- Publication type:
- Article
Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma.
- Published in:
- 2019
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- Publication type:
- journal article
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia.
- Published in:
- G3: Genes | Genomes | Genetics, 2017, v. 7, n. 10, p. 3257, doi. 10.1534/g3.117.300109
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- Publication type:
- Article
The genetic and clinical landscape of nanophthalmos and posterior microphthalmos in an Australian cohort.
- Published in:
- Clinical Genetics, 2020, v. 97, n. 5, p. 764, doi. 10.1111/cge.13722
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- Publication type:
- Article
Improving parents' knowledge of early signs of paediatric eye disease: A double‐blind randomized controlled trial.
- Published in:
- Clinical & Experimental Ophthalmology, 2020, v. 48, n. 9, p. 1250, doi. 10.1111/ceo.13866
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- Publication type:
- Article
Clinical and molecular characterization of females affected by X-linked retinoschisis.
- Published in:
- Clinical & Experimental Ophthalmology, 2015, v. 43, n. 7, p. 643, doi. 10.1111/ceo.12541
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- Publication type:
- Article
Incidence and predictors of glaucoma following surgery for congenital cataract in the first year of life in Victoria, Australia.
- Published in:
- Clinical & Experimental Ophthalmology, 2013, v. 41, n. 7, p. 653, doi. 10.1111/ceo.12067
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- Publication type:
- Article
Familial retinal detachment associated with COL2A1 exon 2 and FZD4 mutations.
- Published in:
- Clinical & Experimental Ophthalmology, 2012, v. 40, n. 5, p. 476, doi. 10.1111/j.1442-9071.2012.02804.x
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- Publication type:
- Article
Telemedicine model to prevent blindness from familial glaucoma.
- Published in:
- Clinical & Experimental Ophthalmology, 2011, v. 39, n. 8, p. 760, doi. 10.1111/j.1442-9071.2011.02556.x
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- Publication type:
- Article
Rock, paper and scissors? Traumatic paediatric cataract in Victoria 1992–2006.
- Published in:
- Clinical & Experimental Ophthalmology, 2010, v. 38, n. 3, p. 237, doi. 10.1111/j.1442-9071.2010.02236.x
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- Publication type:
- Article
Managing fetuses at high risk of retinoblastoma: lesion detection on screening MRI.
- Published in:
- Prenatal Diagnosis, 2015, v. 35, n. 2, p. 174, doi. 10.1002/pd.4514
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- Publication type:
- Article