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Defect
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RNDr. Eduard Kočárek Ph.D.
Academic staff at Second Faculty of Medicine
10 classes
55 publications
Classes
class
Molecular Cytogenetics
D01000132 |
Second Faculty of Medicine
class
Examination Methods in Medical Cytogenetics
D0600022 |
Second Faculty of Medicine
class
Genetics and Molecular Biology II
D0605044 |
Second Faculty of Medicine
class
Medical Biology
D0801003 |
Second Faculty of Medicine
class
Biology
D1301035 |
Second Faculty of Medicine
class
Basics of Genetics and Prenatal Diagnostics
+1
D19010005 |
Second Faculty of Medicine
class
OS - Examination Methods in Medical Genetics
+1
DV01077 |
Second Faculty of Medicine
class
OS - Geographical Medicine
DV01078 |
Second Faculty of Medicine
Publications
publication
anamnézy; defekt jednoho genu
2006 |
Second Faculty of Medicine, Central Library of Charles University, First Faculty of Medicine, Faculty of Physical Education and Sport, Third Faculty of Medicine
publication
Prader-Willi syndrome due to uniparental disomy in a patient with a balanced chromosomal translocation
2006 |
Second Faculty of Medicine
publication
Early development of immunity in diGeorge syndrome
2005 |
Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
publication
Chromosomal examination in medicine
2002 |
Second Faculty of Medicine
publication
Relationship between Genotype and Phenotype in Patients with Microdeletion of Chromosome 22q11
2001 |
Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
publication
Williams-Beuren syndrome
2000 |
Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
publication
Chromosomal Aberration in Inborn Cardiac Defects and their Diagnosis Using the FISH Method
1999 |
Second Faculty of Medicine
publication
Two supernumerary marker-chromosomes in a healthy woman: a case report
Publication without faculty affiliation
publication
Two supernumerary marker-chromosomes in a healthy woman - a case report
Publication without faculty affiliation
publication
A boy with developmental delay and mosaic supernumerary inv dup(5)(p15.33p15.1) leading to distal 5p tetrasomy - case report and review of the literature
2018 |
Second Faculty of Medicine
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