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Array CGH
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Detection of chromosome changes by CGH, array-CGH and SNP array techniques in tumours
2014 |
First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
publication
Case of 12q24.31 Interstitial Deletion in Association with Intellectual Disability, Dysmorphic Features and Short Stature
2013 |
Publication without faculty affiliation
publication
Cytogenetics
2013 |
Publication without faculty affiliation
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
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
Chromophobe renal cell carcinoma - chromosomal aberration variability and its relation to Paner grading system: an array CGH and FISH analysis of 37 cases
2013 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Genetická diagnostika epilepsií ve FN Motol aneb význam detekce CNVs pomocí metody array CGH
2019 |
Second Faculty of Medicine
publication
An inherited 2q13 deletion in a patient with Marfan syndrome
Publication without faculty affiliation
publication
Molecular genetic analysis in 14 Czech Kabuki syndrome patients is confirming the utility of phenotypic scoring
2016 |
First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine, Faculty of Medicine in Hradec Králové
publication
True monozomy of chromosome 5 is presumably not an isolated cytogenetic entity in myelodysplastic syndromes (MDS).
Publication without faculty affiliation
publication
Diagnostic implications of genetic copy number variation in epilepsy plus
2019 |
Second Faculty of Medicine
publication
Molecular cloning and analysis of breakpoints on ring chromosome 17 in a patient with autism
2008 |
Second Faculty of Medicine
publication
FMR1 Gene Expansion, Large Deletion of Xp, and Skewed X-Inactivation in a Girl With Mental Retardation and Autism
2010 |
Second Faculty of Medicine
publication
"Mucin"-secreting papillary renal cell carcinoma: clinicopathological, immunohistochemical, and molecular genetic analysis of seven cases
2016 |
Faculty of Medicine in Pilsen
publication
FMR1 Gene Expansion, Large Deletion of Xp, and Skewed X-Inactivation in a Girl With Mental Retardation and Autism
2010 |
First Faculty of Medicine
publication
Complex cytogenetic and molecular genetic diagnostics of congenital heart defects
Publication without faculty affiliation
publication
Utilization of MLPA to detection of genetic changes in neuroblastoma
2008 |
Second Faculty of Medicine
publication
Cardiogenetics through cytogenetic eyes - submicroscopic aberration in patients with congenital heart defects
2018 |
Second Faculty of Medicine
publication
Delece 18p v mozaice u pacienta s fenotypem připomínajícím syndrom Noonanové
2016 |
First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine, Faculty of Mathematics and Physics
publication
Interstitial del(14)(q) involving IGH: a novel recurrent aberration in B-NHL (1)
2007 |
First Faculty of Medicine
publication
Interstitial del(14)(q) involving IGH: a novel recurrent aberration in B-NHL (1)
2007 |
Faculty of Physical Education and Sport
publication
Delece 2q13 u pacienta s Marfanovým syndromem
2017 |
Faculty of Science, First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
publication
Uterine smooth muscle tumor analysis by comparative genomic hybridization: a useful diagnostic tool in challenging lesions
2015 |
First Faculty of Medicine
publication
Low-grade oncocytic tumour of kidney (CD117-negative, cytokeratin 7-positive): a distinct entity?
2019 |
Faculty of Medicine in Pilsen
publication
A girl with an inherited central deletion 22q11.21 resulting in DiGeorge syndrome without typical congenital anomalies
Publication without faculty affiliation
publication
A girl with an inherited central deletion 22q11.21 resulting in DiGeorge syndrome without typical congenital anomalies
2019 |
Second Faculty of Medicine, Central Library of Charles University
publication
The clinical utility of optical genome mapping for the assessment of genomic aberrations in acute lymphoblastic leukemia
2021 |
Second Faculty of Medicine
publication
Molecular Cytogenetic Characterization in Four Pediatric Pheochromocytomas and Paragangliomas
2011 |
Faculty of Science, First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
publication
Czech and Slovak Diamond-Blackfan Anemia (DBA) Registry update: Clinical data and novel causative genetic lesions
2020 |
Central Library of Charles University