28 results on '"Pater, John"'
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2. Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma
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3. Pathogenic genetic variants identified in Australian families with paediatric cataract
4. 7. MUTATION SPECTRUM OF PRIMARY CONGENITAL GLAUCOMA IN THE AUSTRALIAN AND NEW ZEALAND REGISTRY OF ADVANCED GLAUCOMA: 1907
5. Complications of Limbal Stay Sutures in Strabismus Surgery
6. Paediatric endoscopic endonasal dacryocystorhinostomy in congenital nasolacrimal duct obstruction
7. Identification of a Novel Oligomerization Disrupting Mutation in CRYAA Associated with Congenital Cataract in a South Australian Family
8. Case series of cat-scratch-inflicted full-thickness corneal lacerations and a review of the literature
9. A Novel Genetic Syndrome Characterized by Pediatric Cataract, Dysmorphism, Ectodermal Features, and Developmental Delay in an Indigenous Australian Family
10. Are long-chain polyunsaturated fatty acids essential nutrients in infancy?
11. Prevalence ofFOXC1Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
12. Congenital glaucoma with anterior segment dysgenesis in individuals with biallelicCPAMD8variants
13. MOESM1 of Recurrent mutation in the crystallin alpha A gene associated with inherited paediatric cataract
14. Erratum: Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants
15. High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia
16. Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants
17. Congenital orbital teratoma
18. Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma.
19. Partial duplication of the CRYBB1-CRYBA4 locus is associated with autosomal dominant congenital cataract
20. An exegetical commentary on Psalm 103
21. Partial duplication of the CRYBB1-CRYBA4 locus is associated with autosomal dominant congenital cataract
22. Recurrent mutation in the crystallin alpha A gene associated with inherited paediatric cataract
23. Identification of a Novel Oligomerization Disrupting Mutation inCRYΑAAssociated with Congenital Cataract in a South Australian Family
24. Terson Syndrome from a Significant Cerebral Infarct Occurring During the Peripartum Period
25. Endoscopic Drainage of a Superiorly Based Subperiosteal Orbital Abscess
26. Blinding Orbital Cellulitis: A Complication of Strabismus Surgery
27. Identification of a novel oligomerization disrupting mutation in CRYΑA associated with congenital cataract in a South Australian family
28. Terson Syndrome from a Significant Cerebral Infarct Occurring During the Peripartum Period.
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