A recurrent deletion on chromosome 2q13 is associated with developmental delay and mild facial dysmorphisms
2015 · Molecular Cytogenetics · 66 citations
https://doi.org/10.1186/s13039-015-0157-0
V
Vladimíra Vallová
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Vladimíra Vallová is an academic researcher from Masaryk University. The author has contributed to research in topics: Genomic variations and chromosomal abnormalities & Genetics and Neurodevelopmental Disorders & Genomics and Rare Diseases. The author has an h-index of 9, co-authored 34 publications.
Papers by this author
worksThe clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay
2019 · BMC Medical Genomics · 32 citations
https://doi.org/10.1186/s12920-019-0559-7
Exome sequencing improves the molecular diagnostics of paediatric unexplained neurodevelopmental disorders
2024 · Orphanet Journal of Rare Diseases · 12 citations
https://doi.org/10.1186/s13023-024-03056-6
Additional file 1: of The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay
2019 · Figshare · 0 citations
https://doi.org/10.6084/m9.figshare.8989841
Additional file 4: of The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay
2019 · Figshare · 0 citations
https://doi.org/10.6084/m9.figshare.8989862
Additional file 6: of The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay
2019 · Figshare · 0 citations
https://doi.org/10.6084/m9.figshare.8989874
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