Show
Sort by
-
Copy number analysis of ABCA4 in Belgian patients with Stargardt reveals exon 20-22 deletion
-
Copy number analysis of ABCA4 in Belgian patients with Stargardt reveals exon 20-22 deletion
-
Identity-by-descent-guided mutation analysis and exome sequencing in consanguineous families reveals unusual clinical and molecular findings in retinal dystrophy
-
Identity-by-descent mapping and exome sequencing reveals a new candidate gene for the primary congenital glaucoma locus GLC3E
-
A dual approach for comprehensive genetic testing of ABCA4 in Stargardt disease
-
A dual approach for comprehensive genetic testing of ABCA4 in Stargardt disease
-
Copy number analysis of ABCA4 in Belgian patients with Stargardt reveals exon 20-22 deletion
-
A dual approach for comprehensive genetic testing of ABCA4 in Stargardt disease
-
A dual approach for comprehensive genetic testing of ABCA4 in Stargardt disease
-
Massively parallel sequencing for early molecular diagnosis in Leber congenital amaurosis
-
Identity-by-descent mapping reveals a new locus for primary congenital glaucoma, GLC3E, on chromosome 19p13.2
-
DNA-chipanalyse in de moleculaire diagnostiek van genetisch heterogene aandoeningen : netvliesaandoeningen als voorbeeld
-
CEP290, a gene with many faces : mutation overview and presentation of CEP290base