Diagnostic Single Gene Analyses Beyond Sanger
Najm, J.; Rath, M.; Schröder, W.; Felbor, U. · Zeitschrift für Orthopädie und Unfallchirurgie · 2018 · Heft 03 · S. 158 bis 165
Bibliografische Angaben
Zusammenfassung
SummaryMolecular testing of congenital coagulation and platelet disorders offers confirmation of clinical diagnoses, supports genetic counselling, and enables predictive and prenatal diagnosis. In some cases, genotype-phenotype correlations are important for predicting the clinical course of the disease and adaptation of individualized therapy. Until recently, genotyping has been mainly performed by Sanger sequencing. While next generation sequencing (NGS) enables the parallel analysis of multiple genes, the cost-value ratio of custom-made panels can be unfavorable for analyses of specific small genes. The aim o…