ℹ️
🇬🇧
Search
Search for publications relevant for "H63D"
H63D
Publication
Class
Person
Publication
Programmes
Export current view
publication
The importance of DNA analysis of C282Y, H63D and S65C mutations in the HFE gene
2012 |
Faculty of Medicine in Hradec Králové
publication
Determination of mutations C282Y and H63D: Presence of healthy population and liver disease
2000 |
First Faculty of Medicine
publication
The prevalence and role of hemochromatosis gene mutations C282Y, H63D, and S65C in patients with systemic rheumatoid disease
2007 |
Faculty of Physical Education and Sport, Third Faculty of Medicine, First Faculty of Medicine
publication
HFE gene mutations in patients with rheumatic diseases
2005 |
Faculty of Physical Education and Sport, Third Faculty of Medicine, First Faculty of Medicine
publication
Hereditary hemochromatosis: Detection of C282Y and H63D mutations in HFE gene by means of guthrie cards in population of Czech Republic
2002 |
Third Faculty of Medicine
publication
Prevalence of HFE gene C282Y and H63D mutations and elevated iron biochemistries in patients with non-alcoholic fatty liver and alcoholic liver disease
2004 |
Third Faculty of Medicine
publication
Clinical significance of heterozygotic mutations of the HFE gene in chronic hepatitis C
2007 |
Third Faculty of Medicine
publication
Prevalence of heterozygous HFE gene mutation in chronic liver disease
2007 |
Third Faculty of Medicine, First Faculty of Medicine
publication
S65C and other mutations in the Haemochromatosis gene in the Czech population
2005 |
Faculty of Physical Education and Sport, Third Faculty of Medicine
publication
Mutation of the HFE gene in patients with hereditary hemochromatosis and other diseases with iron accumulation in the liver
2002 |
Third Faculty of Medicine
publication
Multiplex Dideoxynucleotide Sequencing Using Polyadenylated Sequencing Primers Multiplex Dideoxynucleotide Sequencing Using Polyadenylated Sequencing Primers
2013 |
Faculty of Medicine in Hradec Králové
publication
Iron overload and HFE gene mutations in Czech patients with chronic liver diseases
2012 |
Third Faculty of Medicine
publication
High prevalence of HFE gene mutations in patients with porphyria cutanea tarda in the Czech Republic
2008 |
Third Faculty of Medicine
publication
Thermal stabilisation of the short DNA duplexes by acridine-4-carboxamide derivatives
2022 |
Faculty of Pharmacy in Hradec Králové