Vladimíra Vallová

A recurrent deletion on chromosome 2q13 is associated with developmental delay and mild facial dysmorphisms

Eva Hladílková, Tuva Barøy, Madeleine Fannemel et al. · Molecular Cytogenetics · 2015 · 66 citations · Full text

The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay

Markéta Wayhelová, Jan Smetana, Vladimíra Vallová et al. · BMC Medical Genomics · 2019 · 32 citations · Full text

Genome-Wide Screening of Cytogenetic Abnormalities in Multiple Myeloma Patients Using Array-CGH Technique: A Czech Multicenter Experience

Jan Smetana, Jan Fröhlich, Romana Zaoralová et al. · BioMed Research International · 2014 · 25 citations · Full text

Cytogenetics, Mixed-phenotype Acute Leukemia, Genetics +17

Case Report: Contiguous Xq22.3 Deletion Associated with ATS-ID Syndrome: From Genotype to Further Delineation of the Phenotype

Jan Smetana, Vladimíra Vallová, Markéta Wayhelová et al. · Frontiers in Genetics · 2021 · 19 citations · Full text

Novel de novo pathogenic variant in the GNAI1 gene as a cause of severe disorders of intellectual development

Markéta Wayhelová, Vladimíra Vallová, Petr Brož et al. · Journal of Human Genetics · 2021 · 18 citations