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OR9-001 - Exome sequencing in monogenic Behçet-like diseaseDOI 10.1186/1546-0096-11-s1-a184
Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behçet's Disease.Semantic proximity
Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosisSemantic proximity
Genetic testing of Behçet’s disease using next-generation sequencing to identify monogenic mimics and HLA-B*51Semantic proximity
Exploratory whole-exome sequencing identifies candidate DNA variants in Ocular Behcet disease: a pilot study from a Pakistani cohort.Semantic proximity
NeMO mutations: a rare cause of monogenic Behçet-like disease.Semantic proximity
Exome sequencing and characterization of 49,960 individuals in the UK Biobank.Semantic proximity
A Copernican revolution of multigenic analysis: A retrospective study on clinical exome sequencing in unclear genetic disordersSemantic proximity
Performing whole-exome sequencing in Bardet-Bield syndromeSemantic proximity
Approaches based on miRNAs in Behçet's Disease: Unveiling pathogenic mechanisms, diagnostic strategies, and therapeutic applicationsSemantic proximity
Estimating the relative frequency of leukodystrophies and recommendations for carrier screening in the era of next-generation sequencing.Semantic proximity
Behçet disease, new insights in disease associations and manifestations: a next-generation sequencing study.Semantic proximity
Exome Sequencing and Clinical DiagnosisSemantic proximity
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