Advanced search

Search results

Products found: 30Search results

← Prev 1 2 3 Next →

Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory

Disorder	Genes	Test Method	Lab Info	Product code
ABCA4-Related Retinitis Pigmentosa - Sequence analysis of the entire coding region	Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory	ABCA4-Related Retinitis Pigmentosa				CODE: 22429	Add to Cart Add to Compare List
ABCA4-Related Stargardt Disease 1 - Sequence analysis of the entire coding region	Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory	ABCA4-Related Stargardt Disease 1	ABCA4,			CODE: 22430	Add to Cart Add to Compare List
Best Vitelliform Macular Dystrophy - Sequence analysis of the entire coding region	Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory	Best Vitelliform Macular Dystrophy	BEST1,			CODE: 22431	Add to Cart Add to Compare List
CACNA1F-Related X-Linked Congenital Stationary Night Blindness - Sequence analysis of the entire coding region	Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory	CACNA1F-Related X-Linked Congenital Stationary Night Blindness	CACNA1F,			CODE: 22432	Add to Cart Add to Compare List
Cone-Rod Dystrophy 3 - Mutation scanning of the entire coding region	Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory	Cone-Rod Dystrophy 3	ABCA4,	Mutation scanning of the entire coding region		CODE: 22434	Add to Cart Add to Compare List
Cone-Rod Dystrophy 3 - Sequence analysis of the entire coding region	Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory	Cone-Rod Dystrophy 3	ABCA4,			CODE: 22433	Add to Cart Add to Compare List
Congenital Stationary Night Blindness, Type 1B - Sequence analysis of the entire coding region	Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory	Congenital Stationary Night Blindness, Type 1B	GRM6,			CODE: 22435	Add to Cart Add to Compare List
Congenital Stationary Night Blindness, Type 1C - Sequence analysis of the entire coding region	Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory	Congenital Stationary Night Blindness, Type 1C	TRPM1,			CODE: 22436	Add to Cart Add to Compare List
Congenital Stationary Night Blindness, Type 2B - Sequence analysis of the entire coding region	Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory	Congenital Stationary Night Blindness, Type 2B	CABP4,			CODE: 22437	Add to Cart Add to Compare List
CRB1-Related Leber Congenital Amaurosis - Sequence analysis of the entire coding region	Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory	CRB1-Related Leber Congenital Amaurosis				CODE: 22438	Add to Cart Add to Compare List
CRB1-Related Retinitis Pigmentosa - Sequence analysis of the entire coding region	Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory	CRB1-Related Retinitis Pigmentosa				CODE: 22439	Add to Cart Add to Compare List
CYP1B1-Related Primary Congenital Glaucoma - Sequence analysis of the entire coding region	Netherlands Institute for Neuroscience, Molecular Ophthalmogenetics Laboratory	CYP1B1-Related Primary Congenital Glaucoma				CODE: 22440	Add to Cart Add to Compare List

← Prev 1 2 3 Next →

Loading...