ℹ️
🇬🇧
Search
Search for publications relevant for "Genotype and Phenotype"
Genotype and Phenotype
Publication
Class
Person
Publication
Programmes
Export current view
publication
The Correlation of Genotype and Phenotype in Children with Autosomal Dominant Polycystic Kidney Disease
Publication without faculty affiliation
publication
Correlation of genotypes and phenotypes in patients with Duchenne and Becker muscular dystrophy caused by deletions in the dystrophine gene
2002 |
Publication without faculty affiliation
publication
The comparison of genotype and phenotype of some biomechaniclly important bone dysplasias
2002 |
First Faculty of Medicine
publication
Relationship between Genotype and Phenotype in Patients with Microdeletion of Chromosome 22q11
2001 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation
2016 |
Second Faculty of Medicine
publication
Integrative Study of Genotypic and Phenotypic Diversity in the Eurasian Orchid Genus Neotinea
2021 |
Faculty of Science, Central Library of Charles University
publication
Genotypic and phenotypic analysis of HIV-1 protease from Czech patients treated with protease inhibitors : towards a multipotent protease inhibitor
2000 |
First Faculty of Medicine
publication
The molecular basis of medium-chain acyl-CoA dehydrogenase /MCAD/ deficiency in compound heterozygous patients - is there correlation between genotype and phenotype.
1997 |
Faculty of Physical Education and Sport
publication
Genotypic and phenotypic characterization of the Acinetobacter calcoaceticus-Acinetobacter baumannii complex with the proposal of Acinetobacter pittii sp nov (formerly Acinetobacter genomic species 3) and Acinetobacter nosocomialis sp nov (formerly Acinetobacter genomic species 13TU)
2011 |
Faculty of Science
publication
Osteogenesis imperfecta syndrome: Evalution of the effect of mutations on phenotype
Publication without faculty affiliation
publication
Collagen type I gene mutations of alpha 1 chain (Col1A1) in Czech patients with Osteogenesis Imperfecta Syndrome
2003 |
Faculty of Science
publication
Collagen type I gene mutations of alpha 1 chain (Col1A1) in Czech patients with Osteogenesis Imperfecta Syndrome
2003 |
First Faculty of Medicine, Faculty of Mathematics and Physics
publication
Emergence of living language: Ontogeny - phylogeny framework and other parallels of linguistics and biology
2018 |
Faculty of Science
publication
Classification and genetics of cardiomyopathies
2011 |
Publication without faculty affiliation
publication
Latent obstruction in outflow tract of left ventricle in patient with hypertrophic cardiomyopathy
2011 |
Third Faculty of Medicine
publication
Comparing Bioinformatic Gene Expression Profiling Methods: Microarray and RNA-Seq
2014 |
First Faculty of Medicine, Second Faculty of Medicine
publication
The genetics of cardiomyopathies
2010 |
Publication without faculty affiliation
publication
Genetics of cardiomyopathies
2015 |
Publication without faculty affiliation
publication
Epidemiological characteristics of methicillin-resistant Staphylococcus aureus isolates from bloodstream cultures at University Hospital in the Czech Republic
2020 |
Third Faculty of Medicine, Faculty of Medicine in Hradec Králové
publication
Primary ciliary dyskinesia - detection and diagnostic protocol for adult patients
2021 |
First Faculty of Medicine, Second Faculty of Medicine, Central Library of Charles University
publication
Diagnostic possibilities of Prader-Willi and of Angelman syndromes
2005 |
Second Faculty of Medicine
publication
Alagille syndrome
2014 |
Second Faculty of Medicine
publication
Whole-Exome Sequencing in Czech Patients with Neurogenetic Diseases
2020 |
Second Faculty of Medicine
publication
Biotechnological Conversion of Grape Pomace to Poly(3-hydroxybutyrate) by Moderately Thermophilic Bacterium Tepidimonas taiwanensis
2021 |
Publication without faculty affiliation
publication
Anophthalmia, hearing loss, abnormal pituitary development and response to growth hormone therapy in three children with microdeletions of 14q22q23
2014 |
Second Faculty of Medicine
publication
Association of candidate pharmacogenetic markers with platinum-induced ototoxicity: PanCareLIFE dataset
2020 |
Second Faculty of Medicine
publication
Characterisation of ATM mutations in Slavic Ataxia telangiectasia patients
2011 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Characterisation of ATM Mutations in Slavic Ataxia Telangiectasia Patients
2011 |
Second Faculty of Medicine
publication
Whole genome sequencing of a clinical drug resistant Candida albicans isolate reveals known and novel mutations in genes involved in resistance acquisition mechanisms
2021 |
Faculty of Medicine in Pilsen, Central Library of Charles University
publication
Adaptive differentiation of Festuca rubra along a climate gradient revealed by molecular markers and quantitative traits
2018 |
Faculty of Science