Sort   by:  
 Page size 
UnknownTargeted next generation sequencing identifies novel mutations in RP1 as a relatively common cause of autosomal recessive rod-cone dystrophy.
Not available
S-EPMC4307388 | biostudies-literature
UnknownPhenotype Analysis of Retinal Dystrophies in Light of the Underlying Genetic Defects: Application to Cone and Cone-Rod Dystrophies.
Not available
S-EPMC6801687 | biostudies-literature
UnknownNext-generation sequencing applied to a large French cone and cone-rod dystrophy cohort: mutation spectrum and new genotype-phenotype correlation.
Not available
S-EPMC4566196 | biostudies-literature
UnknownRetinal Phenotype of Patients With Isolated Retinal Degeneration Due to CLN3 Pathogenic Variants in a French Retinitis Pigmentosa Cohort.
Not available
S-EPMC7844693 | biostudies-literature
UnknownWhole-exome sequencing identifies KIZ as a ciliary gene associated with autosomal-recessive rod-cone dystrophy.
Not available
S-EPMC3980423 | biostudies-literature
Sort   by:  
 Page size