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3. Tissue-specific TCF4 triplet repeat instability revealed by optical genome mapping

4. Lisch Epithelial Corneal Dystrophy Is Caused by Heterozygous Loss-of-Function Variants in MCOLN1

6. A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus.

10. Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease

12. Tissue-Specific Dynamics of TCF4 Triplet Repeat Instability Revealed by Optical Genome Mapping

15. Mutations in CPAMD8 Cause a Unique Form of Autosomal-Recessive Anterior Segment Dysgenesis

28. Wet Lab

29. Refractive Corneal Surgery

30. Corneal Transplantation

31. Introduction

33. Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease

34. Phenotype and genotype of concurrent keratoconus and Fuchs endothelial corneal dystrophy

36. Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2

38. Autosomal dominant stromal corneal dystrophy associated with a SPARCL1missense variant

45. List of Contributors

49. Personalized Model to Predict Keratoconus Progression From Demographic, Topographic, and Genetic Data

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