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Search for publications relevant for "molecular genetics"
molecular genetics
Publication
Class
Person
Publication
Programmes
publication
Perspectives of molecular genetic methods
Publication without faculty affiliation
publication
Myotonic dystrophies
2012 |
Second Faculty of Medicine
publication
Cytogenetic and molecular genetic methods
2010 |
Publication without faculty affiliation
publication
Molecular genetics for bioanalysts
2016 |
Faculty of Medicine in Hradec Králové, Faculty of Pharmacy in Hradec Králové
publication
Molecular genetic cause of X-linked retinitis pigmentosa in a Czech family
2011 |
First Faculty of Medicine
publication
An update on immunohistochemical and molecular genetic markers of selected soft tissue tumors
2021 |
Faculty of Medicine in Pilsen
publication
Monogenic obesity - current status of molecular genetic research and clinical importance
2014 |
Third Faculty of Medicine
publication
A standardized framework for the validation and verification of clinical molecular genetic tests
2010 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Molecular genetics of renal cell tumors: A practical diagnostic approach
2020 |
Faculty of Medicine in Pilsen
publication
Cyto- and molecular genetic abnormality differences between children < 2 years and older with acute myeloid leukemia
Publication without faculty affiliation
publication
First Molecular Genetic Characterization of Skene's Gland Adenocarcinoma
2021 |
Faculty of Medicine in Pilsen
publication
Practices recommendations in the applications of immunohistochemistry and molecular genetics in testicular tumors. Review article
2020 |
Faculty of Medicine in Pilsen
publication
Introduction of molecular genetic diagnosis in syndromes with a hearing defect
1998 |
Second Faculty of Medicine
publication
Differences in cyto- and molecular genetic aberrations between young (<2YR) and older children with acute myeloid leukemia
Publication without faculty affiliation
publication
Renal angiomyoadenomatous tumor: morphologic, immunohistochemical, and molecular genetic study of a distinct entity
2009 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Possibilities of molecular genetic determination of age of an individual from biological traces
2014 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Aetiology of childhood ALL and AML, molecular genetics and minimal residual disease
2015 |
Second Faculty of Medicine
publication
Molecular genetics of dyslipidemia
2009 |
First Faculty of Medicine
publication
X-linked Hypogammaglobulinaemia (Bruton´s Disease) - Three Case Studies and Molecular Genetic Studies in Their Families
2004 |
First Faculty of Medicine
publication
Immunohistochemistry and molecular genetics in the differential diagnostics of mesenchymal lesions of gastrointestinal tract
2020 |
Faculty of Medicine in Pilsen
publication
Molecular Genetic Testing of Diabetes Insipidus Renalis
2019 |
Faculty of Medicine in Pilsen
publication
The basic knowledge of varicella zoster virus (VZV) molecular genetic testing
2017 |
Faculty of Medicine in Hradec Králové
publication
Myxoinflammatory fibroblastic sarcoma: an immunohistochemical and molecular genetic study of 73 cases
2020 |
Faculty of Medicine in Pilsen
publication
Hereditary Neuropathy
2010 |
Second Faculty of Medicine
publication
Implication of molecular genetic examination in a three generational family with multiple endocrine neoplasia type 2A
2007 |
Faculty of Medicine in Hradec Králové
publication
Implication of molecular genetic examination in a three generational family with multiple endocrine neoplasia type 2A
2007 |
Faculty of Medicine in Hradec Králové, Central Library of Charles University
publication
Implication of molecular genetic examination in a three generational family with multiple endocrine neoplasia type 2A
2007 |
Faculty of Medicine in Hradec Králov é, First Faculty of Medicine, Central Library of Charles University, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Implication of molecular genetic examination in a three generational family with multiple endocrine neoplasia type 2A
2007 |
First Faculty of Medicine
publication
Molecular genetics of myocardial infarction
2007 |
First Faculty of Medicine
publication
Molecular Genetics of Huntington´s Disease
2000 |
Publication without faculty affiliation