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Publications by G. A. Gole
Familial Exudative Vitreoretinopathy
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
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Familial Exudative Vitreoretinopathy
101 Familial Exudative Vitreoretinopathy
Recessive Mutations inTSPAN12Cause Retinal Dysplasia and Severe Familial Exudative Vitreoretinopathy (FEVR)
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Identification of Novel KIF11 Mutations in Patients With Familial Exudative Vitreoretinopathy and a Phenotypic Analysis
Scientific Reports
Multidisciplinary
A Start Codon Mutation of the TSPAN12 Gene in Chinese Families Causes Clinical Heterogeneous Familial Exudative Vitreoretinopathy
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Genetic Heterogeneity in Familial Exudative Vitreoretinopathy; Exclusion of the EVR1 Locus on Chromosome 11q in a Large Autosomal Dominant Pedigree
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Overview of the Mutation Spectrum in Familial Exudative Vitreoretinopathy and Norrie Disease With Identification of 21 Novel Variants in FZD4, LRP5, and NDP
Human Mutation
Genetics
Causal Diagnosis of Familial Exudative Vitreoretinopathy in Two Asymptomatic Siblings. Wide-Field Image Study of Retinal Abnormalities Observed in the Posterior Pole
Revista Mexicana de Oftalmologia
Ophthalmology
Familial Neonatal Hypoproteinaemia With Exudative Enteropathy and Intestinal Lymphangiectasis.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
