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Publications by Jinyue Bai
A Start Codon Mutation of the TSPAN12 Gene in Chinese Families Causes Clinical Heterogeneous Familial Exudative Vitreoretinopathy
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Related publications
Familial Exudative Vitreoretinopathy
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
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
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
Identification of Novel KIF11 Mutations in Patients With Familial Exudative Vitreoretinopathy and a Phenotypic Analysis
Scientific Reports
Multidisciplinary
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
A Point Mutation in the Albumin Gene in a Chinese Patient With Familial Dysalbuminemic Hyperthyroxinemia
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
A Stop Codon Mutation in SCN9A Causes Lack of Pain Sensation
Human Molecular Genetics
Medicine
Genetics
Molecular Biology
