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Association of PEDF polymorphisms with age-related macular degeneration and polypoidal choroidal vasculopathy: a systematic review and meta-analysis.
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- Scientific Reports, 2015, p. 9497, doi. 10.1038/srep09497
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- Article
Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of C0L8A2 mutations in Fuchs endothelial corneal dystrophy.
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- Journal of Human Genetics, 2014, v. 59, n. 8, p. 444, doi. 10.1038/jhg.2014.55
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- Article
Transforming Growth Factor β-1 -509C>T Polymorphism in Indian Patients with Primary Open Angle Glaucoma.
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- Molecular Diagnosis & Therapy, 2007, v. 11, n. 3, p. 151, doi. 10.1007/BF03256236
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- Article
Retinoblastoma in India.
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- Molecular Diagnosis & Therapy, 2007, v. 11, n. 1, p. 63, doi. 10.1007/BF03256223
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- Article
Current concepts and molecular mechanisms in pharmacogenetics of essential hypertension.
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- Indian Journal of Pharmacology, 2021, v. 53, n. 4, p. 301, doi. 10.4103/ijp.IJP_593_19
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- Article
Molecular Mechanisms of Antifungal Drug Resistance in Candida Species.
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- Journal of Clinical & Diagnostic Research, 2018, v. 12, n. 9, p. 1, doi. 10.7860/JCDR/2018/36218.11961
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- Article
Inherited retinal disorders: a genotype–phenotype correlation in an Indian cohort and the importance of genetic testing and genetic counselling.
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- Graefe's Archive of Clinical & Experimental Ophthalmology, 2023, v. 261, n. 7, p. 2003, doi. 10.1007/s00417-022-05955-5
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- Article
Ophthatome™: an integrated knowledgebase of ophthalmic diseases for translating vision research into the clinic.
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- 2020
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- Publication type:
- journal article
Aerobic Bacterial Pathogens causing Vaginitis in Patients Attending A Tertiary Care Hospital and their Antibiotic Susceptibility Pattern.
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- Journal of Pure & Applied Microbiology, 2019, v. 13, n. 2, p. 1169, doi. 10.22207/JPAM.13.2.56
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- Article
The Relationship Between Tumor Cell Differentiation and Age at Diagnosis in Retinoblastoma.
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- Journal of Pediatric Ophthalmology & Strabismus, 2008, v. 45, n. 1, p. 22, doi. 10.3928/01913913-20080101-16
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- Article
Two novel missense substitutions in the VSX1 gene: clinical and genetic analysis of families with Keratoconus from India.
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- BMC Medical Genetics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12881-015-0178-x
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- Article
Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2).
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- Human Mutation, 2007, v. 28, n. 5, p. 522, doi. 10.1002/humu.9487
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- Article
Two Indian siblings with Oguchi disease are homozygous for an arrestin mutation encoding premature termination.
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- Human Mutation, 1998, v. 11, p. S317, doi. 10.1002/humu.1380110199
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- Article
Retinoblastoma: From Disease to Discovery.
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- Ophthalmic Research, 2008, v. 40, n. 5, p. 221, doi. 10.1159/000128578
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- Article
Diabetic Retinopathy and IGF-1Gene Polymorphic Cytosine-Adenine Repeats in a Southern Indian Cohort.
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- Ophthalmic Research, 2007, v. 39, n. 5, p. 294, doi. 10.1159/000108124
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- Publication type:
- Article
Prenatal genetic diagnosis of retinoblastoma--clinical correlates on follow-up.
- Published in:
- 2015
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- Publication type:
- journal article
Genetic and genomic perspective to understand the molecular pathogenesis of keratoconus.
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- 2013
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- Publication type:
- journal article
Genetic and genomic perspective to understand the molecular pathogenesis of keratoconus.
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- Indian Journal of Ophthalmology, 2013, v. 61, n. 8, p. 384, doi. 10.4103/0301-4738.116055
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- Article
Genetic analysis of adult-onset cataract in a city-based ophthalmic hospital.
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- Clinical Genetics, 1997, v. 52, n. 6, p. 427, doi. 10.1111/j.1399-0004.1997.tb02563.x
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- Article
Identification of Novel Mutations in ABCA4 Gene: Clinical and Genetic Analysis of Indian Patients with Stargardt Disease.
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- BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/940864
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- Article
Correlation between tear levels of vascular endothelial growth factor and vitamin D at retinopathy of prematurity stages in preterm infants.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-43338-w
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- Publication type:
- Article
Correlation between tear levels of vascular endothelial growth factor and vitamin D at retinopathy of prematurity stages in preterm infants.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-43338-w
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- Publication type:
- Article
Linkage of Blepharophimosis Syndrome in a Large Indian Pedigree to Chromosome 7p.
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- Human Molecular Genetics, 1996, v. 5, n. 12, p. 2049, doi. 10.1093/hmg/5.12.2049
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- Article
Retinoblastoma genetics screening and clinical management.
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- BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-01034-6
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- Article