Publikationen 2018
Braunisch MC, Büttner-Herold M, Günthner R, Satanovskij R, Riedhammer KM, Herr PM, Klein HG, Wahl D, Küchle C, Renders L, Heemann U, Schmaderer C, Hoefele J
Heterozygous COL4A3 Variants in Histologically Diagnosed Focal Segmental Glomerulosclerosis
Front. Pediatr. | doi: 10.3389/fped.2018.00171
Kraus T,
Emergence of exosomal DNA in molecular neuropathology
J Lab Med 42(1–2): 9 (2018)
Bauer P, Wildhardt G, Gläser D, Müller-Reible C, Bolz H, Klein HG, Finckh U, Hehr U,
German Guidelines for Molecular Genetic Diagnostic Testing Using High-throughput Technology, Such As Next-Generation Sequencing
OBM Genetics SSN 2577-5790 (2018)
Dincer Y, Schulz J, Wilson S, Marschall C, Cohen M, Mall V, Klein HG, Eck S,
Multiple Integration and Data Annotation Study (MIDAS): improving next-generation sequencing data analysis by genotype-phenotype correlations
J Lab Med 42(1–2): 1 (2018)