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Ceskoslovenska Patologie|July 19, 2023
Molecular diagnosis of complete and partial hydatidiform molesMartina Putzová, Šárka Hadravská, Magdaléna DaumováCeskoslovenska Patologie|July 19, 2023
Hydatidiform moleMagdaléna Daumová, Šárka Hadravská, Martina PutzováCeskoslovenska Patologie|July 19, 2023
Spontaneous abortion in the first trimester of pregnancyMagdaléna Daumová, Šárka Hadravská, Martina PutzováMedicina Clinica|August 12, 2017
Preimplantation genetic diagnosis of X-linked Charcot-Marie-Tooth disease by indirect linkage analysisIrena Borgulová, Martina Putzová, Inna Soldatova, et al.Journal of Human Genetics|April 12, 2018
Genome-wide uniparental diploidy of all paternal chromosomes in an 11-year-old girl with deafness and without malignancyIrena Borgulová, Inna Soldatova, Martina Putzová, et al.Journal of Human Genetics|June 24, 2016
SPAST mutation spectrum and familial occurrence among Czech patients with pure hereditary spastic paraplegiaAnna Uhrová Mészárosová, Martina Putzová, Marie Čermáková, et al.Virchows Archiv : an International Journal of Pathology|March 16, 2024
Multicenter evaluation of an automated, multiplex, RNA-based molecular assay for detection of ALK, ROS1, RET fusions and MET exon 14 skipping in NSCLCLinea Melchior, Astrid Hirschmann, Paul Hofman, et al.Frontiers in Medicine|January 3, 2024
The most common founder pathogenic variant c.868G > A (p.Val290Met) in the NPHS2 gene in a representative adult Czech cohort with focal segmental glomerulosclerosis is associated with a milder disease and its underdiagnosis in childhoodDana Thomasová, Michaela Zelinová, Malgorzata Libik, et al.Virchows Archiv : an International Journal of Pathology|November 10, 2020
Multi-center real-world comparison of the fully automated Idylla™ microsatellite instability assay with routine molecular methods and immunohistochemistry on formalin-fixed paraffin-embedded tissue of colorectal cancerAna Velasco, Fatma Tokat, Jesper Bonde, et al.Pageof 1