RNDr. Vladimíra Vallová, Ph.D.
Assistant professor, Section of Genetics and Molecular Biology
Office: bldg. C13/322
Kamenice 753/5
625 00 Brno
Phone: | +420 549 49 5446 |
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E‑mail: |
social and academic networks: |
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Total number of publications: 117
2012
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ArrayCGH characterization of a deletion on 2q13 associated with developmental delay and facial dysmorphism (case report)
Year: 2012, type: Conference abstract
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Initial experience with determination of hTERC and MYCC genes amplification in cervical intraepithelial neoplasia and cervical carcinoma in the Czech Republic
European Oncology and Haematology, year: 2012, volume: 8, edition: 2
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Unique Combination of 22q11 and 14qter Microdeletion Syndromes Detected Using Oligonucleotide Array-CGH
Molecular Syndromology, year: 2012, volume: 2011;2, edition: No. 2, DOI
2011
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Amplification of hTERC (3q26) and MYCC (8q24) genes in correlation with oncogenic human papilloma virus infection in cervical cancer
Year: 2011, type: Conference abstract
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Amplifikace genů hTERC (3q26) a MYCC (8q24)v buňkách napadených lidským papilloma virem
Year: 2011, type: Conference abstract
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Analysis of chromosomal aberrations in patients with mental retardation using array-CGH technique: a single Czech Centre experience
Folia biologica, year: 2011, volume: 2011, edition: 57 No.5
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Deletion of 9p associated with sex reversal: clinical and molecular-cytogenetic analysis of patients
Year: 2011
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Familiální výskyt balancované a nebalancované formy translokace t(1;12) v rodině se dvěma postižnými dětmi
Year: 2011, type: Conference abstract
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Chromosomal analysis of anaplastic ependymoma and diffuse astrocytoma presenting as synchronous primary brain tumors in a child (case report)
Year: 2011, type: Conference abstract
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Low-level copy number changes of MYC genes have a prognostic impact in medulloblastoma
Journal of Neuro-Oncology, year: 2011, volume: 102, edition: 1, DOI