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152. COL1A1andCOL2A1Genes and Myopia Susceptibility: Evidence of Association and Suggestive Linkage to theCOL2A1Locus

154. Replication of the Recessive STBMS1 Locus but with Dominant Inheritance

155. An International Collaborative Family-Based Whole-Genome Linkage Scan for High-Grade Myopia

156. Evaluation of the X-Linked High-Grade Myopia Locus (MYP1) with Cone Dysfunction and Color Vision Deficiencies

160. Myopia: Recent Advances in Molecular Studies; Prevalence, Progression and Risk Factors; Emmetropization; Therapies; Optical Links; Peripheral Refraction; Sclera and Ocular Growth; Signalling Cascades; and Animal Models

163. Myopia: Recent Advances in Molecular Studies; Prevalence, Progression and Risk Factors; Emmetropization; Therapies; Optical Links; Peripheral Refraction; Sclera and Ocular Growth; Signalling Cascades; and Animal Models

164. Familial recurrence ofSOX2anophthalmia syndrome: Phenotypically normal mother with two affected daughters

170. Subtelomeric deletions of chromosome 6p: Molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher?Schinzel (3C) syndrome

177. What is the appropriate age cut-off for cycloplegia in refraction?

179. Sequencing Analysis of the ATOH7 Gene in Individuals with Optic Nerve Hypoplasia.

192. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

193. Whole genome expression profiling of normal human fetal and adult ocular tissues.

194. Genetic contributions to myopic refractive error: Insights from human studies and supporting evidence from animal models.

198. Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations.

199. Genome-Wide Meta-Analysis of Five Asian Cohorts Identifies PDGFRA as a Susceptibility Locus for Corneal Astigmatism.

200. An evidence-based update on myopia and interventions to retard its progression.

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