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Search for publications relevant for "phenotypic variability"
phenotypic variability
Publication
Class
Person
Publication
Programmes
publication
Phenotypic variability of wild Saccharomyces cerevisiae strains and a role of Flo11p in fluffy colony development.
Publication without faculty affiliation
publication
Possible links between phenotypic variability, habitats and connectivity in the killifish Aphaniops stoliczkanus in Northeast Oman
2023 |
Faculty of Science
publication
Acid sphingomyelinase deficiency. Phenotype variability with prevalence of intermediate phenotype in a series of twenty-five Czech and Slovak patients. A multi-approach study
2005 |
First Faculty of Medicine, Faculty of Physical Education and Sport
publication
Stickler syndrome in the Czech Republic: phenotypic variability and genetic heterogeneity
2021 |
Second Faculty of Medicine
publication
ATAD3A-related pontocerebellar hypoplasia: new patients and insights into phenotypic variability
2023 |
First Faculty of Medicine
publication
Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene
2009 |
Second Faculty of Medicine
publication
Phenotypic variability of genera Heterolepa and Gemellides from the Central Paratethys Oligocene and Miocene
1995 |
First Faculty of Medicine, Faculty of Mathematics and Physics
publication
Phenotype Variability in Czech Patients Carrying PAX6 Disease-Causing Variants
2020 |
First Faculty of Medicine
publication
Pendred syndrome in patients with hypothyroidism: genetic diagnosis, phenotypic variability and occurence of phenocopies
2008 |
Faculty of Medicine in Hradec Králové, Second Faculty of Medicine, Third Faculty of Medicine
publication
Low renal but high extrarenal phenotype variability in Schimke immuno-osseous dysplasia
2017 |
Second Faculty of Medicine
publication
Phenotypic Variability in a Large Czech Family with a Dynamin 2-Associated Charcot-Marie-Tooth Neuropathy
2011 |
Second Faculty of Medicine
publication
The Legacy of Sexual Ancestors in Phenotypic Variability, Gene Expression, and Homoeolog Regulation of Asexual Hybrids and Polyploids
2019 |
Faculty of Science
publication
Genomic imprinting analyses identify maternal effects as a cause of phenotypic variability in type 1 diabetes and rheumatoid arthritis
2020 |
Faculty of Medicine in Pilsen
publication
The influence of polymorphism for gene RGS4 (Regulator of G-protein Signaling 4) on regional brain metabolism (18FDG PET) and phenotypic variables in schizophrenia
2009 |
Publication without faculty affiliation
publication
Lysosomal sphingomyelinase deficiency: Phenotype spectrum of the Czech and Slovak patients
2001 |
First Faculty of Medicine
publication
Surgical Treatment of Congenital Cleft Foot - Case Study and Literature Review
2020 |
Faculty of Medicine in Hradec Králové
publication
Phenotype variance of chronic obstructive pulmonary diseasese - summary for clinical practice
2009 |
Faculty of Medicine in Hradec Králové
publication
Phenotype variance of chronic obstructive pulmonary diseasese - summary for clinical practice
2009 |
Faculty of Medicine in Hradec Králové, Central Library of Charles University
publication
Phenotype variance of chronic obstructive pulmonary diseasese - summary for clinical practice
2009 |
First Faculty of Medicine
publication
Biodiversity in a dish – bacteria as an indicator of an organism phenotypic differentiation
2009 |
Faculty of Science, First Faculty of Medicine, Faculty of Mathematics and Physics
publication
Classification and genetics of cardiomyopathies
2011 |
Publication without faculty affiliation
publication
Williams-Beuren syndrome
2000 |
First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
publication
Sex and gender differences in Alzheimer's disease: current challenges and implications for clinical practice : Position paper of the Dementia and Cognitive Disorders Panel of the European Academy of Neurology
2020 |
Second Faculty of Medicine
publication
Myoclonic dystonia phenotype related to a novel calmodulin-binding transcription activator 1 sequence variant
2021 |
First Faculty of Medicine
publication
New and emerging zoophilic dermatophytes in Europe
Publication without faculty affiliation
publication
The genetics of cardiomyopathies
2010 |
Publication without faculty affiliation
publication
Cryptic Chromosomal Rearrangements in Children with Idiopathic Mental Retardation in the Czech Population
2011 |
First Faculty of Medicine
publication
Genetics of cardiomyopathies
2015 |
Publication without faculty affiliation
publication
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling
Publication without faculty affiliation
publication
Cryptic chromosomal rearrangements in children with idiopathic mental retardation in the czech population
2011 |
Faculty of Science, First Faculty of Medicine