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43 results on '"J. Fielding"'

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1. Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic Mechanism

2. The Genetic Confirmation and Clinical Characterization of LOXL3-Associated MYP28: A Common Type of Recessive Extreme High Myopia

8. Aged Nrf2-Null Mice Develop All Major Types of Age-Related Cataracts

10. Patterns of Crystallin Gene Expression in Differentiation State Specific Regions of the Embryonic Chicken Lens

11. Homozygosity Mapping and Genetic Analysis of Autosomal Recessive Retinal Dystrophies in 144 Consanguineous Pakistani Families

12. Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity Screening

13. Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity Screening

16. Hexokinase 1 and Retinitis Pigmentosa: Insights Into the Retina and the Molecule

18. GNAT1Associated with Autosomal Recessive Congenital Stationary Night Blindness

21. Evaluation of SNPs on Chromosome 2p with Primary Open Angle Glaucoma in the South Indian Cohort

23. Overexpression of Human γC-crystallin 5 bp Duplication Disrupts Lens Morphology in Transgenic Mice

24. Mutations in ASCC3L1 on 2q11.2 Are Associated with Autosomal Dominant Retinitis Pigmentosa in a Chinese Family

26. Analysis of Ocular Hypopigmentation inRab38cht/chtMice

27. Screening of the Eight BBS Genes in Tunisian Families: No Evidence of Triallelism

33. Analysis of Ocular Hypopigmentation inRab38cht/chtMice

34. Genetic Heterogeneity in Microcornea-Cataract: Five Novel Mutations inCRYAA,CRYGD, andGJA8

38. Screening of the Eight BBS Genes in Tunisian Families: No Evidence of Triallelism

39. Autosomal Recessive Retinitis Pigmentosa Is Associated with Mutations inRP1in Three Consanguineous Pakistani Families

40. Mutations in βB3-Crystallin Associated with Autosomal Recessive Cataract in Two Pakistani Families

41. A New Locus for Autosomal Recessive Nuclear Cataract Mapped to Chromosome 19q13 in a Pakistani Family

42. A Homozygous Splice Mutation in theHSF4Gene Is Associated with an Autosomal Recessive Congenital Cataract

43. A Nonsense Mutation in the Glucosaminyl (N-acetyl) Transferase 2 Gene (GCNT2): Association with Autosomal Recessive Congenital Cataracts

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