Items where authors include "Fernandez-Fuentes, N"

Article

Panagiotou, ES, Fernandez-Fuentes, N, Farraj, LA et al. (10 more authors) (2022) Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia. Molecular Vision, 28. pp. 57-69. ISSN 1090-0535

Segura, J, Marín-López, MA, Jones, PF et al. (2 more authors) (2015) VORFFIP-Driven Dock: V-D²OCK, a Fast and Accurate Protein Docking Strategy. PLoS One, 10 (3). e0118107. ISSN 1932-6203

Khan, K, Logan, CV, McKibbin, M et al. (18 more authors) (2012) Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects. Human Molecular Genetics, 21 (4). pp. 776-783. ISSN 0964-6906