Search

Your search keyword '"Pasutto F"' showing total 11 results

Search Constraints

Start Over You searched for: Author "Pasutto F" Remove constraint Author: "Pasutto F" Topic glaucoma Remove constraint Topic: glaucoma
11 results on '"Pasutto F"'

Search Results

1. Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci.

2. Specifications of the ACMG/AMP variant curation guidelines for myocilin: Recommendations from the clingen glaucoma expert panel.

3. An Assessment of GUCA1C Variants in Primary Congenital Glaucoma.

4. Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression.

5. Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma.

6. Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma.

7. Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity.

8. Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucoma.

9. Genotype-correlated expression of lysyl oxidase-like 1 in ocular tissues of patients with pseudoexfoliation syndrome/glaucoma and normal patients.

10. Mutations in CYP1B1 cause primary congenital glaucoma by reduction of either activity or abundance of the enzyme.

11. Primary congenital glaucoma and Rieger's anomaly: extended haplotypes reveal founder effects for eight distinct CYP1B1 mutations.

Catalog

Books, media, physical & digital resources