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A Diverse Set of Case Presentation Highlight the Power of Whole Genome Sequencing – What Next?

Improved Vanadis® cfDNA Platform for Detection of T13 T18 and T21 and Sex Chromosome Abnormalities

Repeat expansion disorders screening by WGS: strategy and stumbling blocks

Diagnostic Yield and Clinical Utility of Nephrolithiasis and Primary Hyperoxaluaria Sequencing panels

Maryland Permit_US

Comprehensive Clinical Grade Whole Genome Sequencing Significantly Improves Diagnostic Yield in Sick Neonates and Pediatric Suspected of a Genetic Disorder

5X WGS assay as a more sensitive and cost-effective method to replace microarray in a diagnostic setting: Experience from the first 100 cases

Next-Generation Sequencing Testing in Identification and Differential Diagnosis of Hereditary Anemia due to Erythrocyte Membrane Disorders, Enzymopathies and Related Disorders

CAP Certificate of Accreditation_UK

Genomic screening for hereditary cancer syndromes in 22,033 individuals


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