Products found: 30Search results

Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory

Disorder Genes Test Method Lab Info Product code  
Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory ABCA4-Related Retinitis Pigmentosa Sequence analysis of the entire coding region
Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory ABCA4-Related Stargardt Disease 1 ABCA4, Sequence analysis of the entire coding region
Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory Best Vitelliform Macular Dystrophy BEST1, Sequence analysis of the entire coding region
Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory CACNA1F-Related X-Linked Congenital Stationary Night Blindness CACNA1F, Sequence analysis of the entire coding region
Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory Cone-Rod Dystrophy 3 ABCA4, Mutation scanning of the entire coding region
Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory Cone-Rod Dystrophy 3 ABCA4, Sequence analysis of the entire coding region
Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory Congenital Stationary Night Blindness, Type 1B GRM6, Sequence analysis of the entire coding region
Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory Congenital Stationary Night Blindness, Type 1C TRPM1, Sequence analysis of the entire coding region
Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory Congenital Stationary Night Blindness, Type 2B CABP4, Sequence analysis of the entire coding region
Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory CRB1-Related Leber Congenital Amaurosis Sequence analysis of the entire coding region
Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory CRB1-Related Retinitis Pigmentosa Sequence analysis of the entire coding region
Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory CYP1B1-Related Primary Congenital Glaucoma Sequence analysis of the entire coding region
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