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Deletion
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publication
Deletions: What they are and where to place them?
2011 |
Faculty of Mathematics and Physics
publication
Old linguists never die, they only get obligatorily deleted
2006 |
Faculty of Mathematics and Physics
publication
Deletions of 12p in hematological malignancies
2003 |
Second Faculty of Medicine
publication
Parameterized Complexity of Fair Deletion Problems
2017 |
Faculty of Mathematics and Physics
publication
Extinguishment of Criminal Lability and Deletion of a Sentence
2007 |
Faculty of Law
publication
Nature of frequent deletions in CEBPA
2009 |
First Faculty of Medicine
publication
Coreference of Deletions – The Case of Control
2011 |
Faculty of Mathematics and Physics
publication
Deletion of the long arm but not the 5q31 region of chromosome 5 in myeloid malignancies
2012 |
First Faculty of Medicine
publication
Multiclonal monoallelic 13q14 interstitial deletion in chronic lymphocytic leukemia
2013 |
Faculty of Medicine in Pilsen
publication
ASXL1 gene alterations in patients with isolated 20q deletion
2019 |
First Faculty of Medicine
publication
Deletions and node reconstructions in a dependency-based mutlilevel annotation scheme
2015 |
Faculty of Mathematics and Physics
publication
An inherited 2q13 deletion in a patient with Marfan syndrome
Publication without faculty affiliation
publication
The Technology of Digital PCR for Analysis of The Deletion Polymorphism in the GSTM1 Gene
2016 |
Faculty of Medicine in Hradec Králové, Faculty of Pharmacy in Hradec Králové
publication
Combination of molecular cytogenetic techniques in mapping of the atypical 5q deletion in myeloid malignancies
Publication without faculty affiliation
publication
Association of 17q24.2-q24.3 deletions with recognizable phenotype and short telomeres
2018 |
Second Faculty of Medicine
publication
Mechanism and Genotype-Phenotype Correlation of Two Proximal 6q Deletions Characterized Using mBAND, FISH, Array CGH, and DNA Sequencing
2012 |
First Faculty of Medicine
publication
Mechanism and Genotype-Phenotype Correlation of Two Proximal 6q Deletions Characterized Using mBAND, FISH, Array CGH, and DNA Sequencing
Publication without faculty affiliation
publication
Reconstruction of Deletions in a Dependency-based Description of Czech: Selected Issues
2015 |
Faculty of Mathematics and Physics
publication
Early Diagnosis of the Chromosomal Deletion 5q14.2-q21.3 in a Preterm Newborn: Case Report
2013 |
First Faculty of Medicine
publication
Co-deletion of 1p/19q as Prognostic and Predictive Biomarker for Patients in West Bohemia with Anaplastic Oligodendroglioma
2016 |
Faculty of Medicine in Pilsen
publication
Molecular and clinical characterization of two patients with Prader-Willi syndrome and atypical deletions of proximal chromosome 15q
2008 |
Second Faculty of Medicine
publication
DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion
2003 |
Second Faculty of Medicine
publication
Mechanism and Genotype-Phenotype Correlation of Two Proximal 6q Deletions Characterized Using mBAND, FISH, Array CGH, and DNA Sequencing
2012 |
Second Faculty of Medicine
publication
Intragenic NF1 deletions in sinonasal mucosal malignant melanoma
2022 |
Faculty of Medicine in Hradec Králové
publication
Case of 12q24.31 Interstitial Deletion in Association with Intellectual Disability, Dysmorphic Features and Short Stature
2013 |
Publication without faculty affiliation
publication
CCR5 Delta 32 Deletion as a Protective Factor in Czech First-Wave COVID-19 Subjects
2021 |
First Faculty of Medicine
publication
Analysis of common SHOX gene sequence variants and similar to 4.9-kb PAR1 deletion in ISS patients
2014 |
First Faculty of Medicine, Faculty of Science
publication
Lack of deletion of 1p36 in 8 cases of primary adenoid cystic carcinoma of the skin
2019 |
Faculty of Medicine in Pilsen
publication
SNP Array and Phenotype Correlation Shows That FLI1 Deletion Per se is Not Responsible for Thrombocytopenia Development in Jacobsen Syndrome
2012 |
Publication without faculty affiliation
publication
A unique coincidence of a 17q12 deletion and duplication in a Czech family led to a refined genotype–phenotype correlation
2023 |
Second Faculty of Medicine