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Search for publications relevant for "human genetic-disease"
human genetic-disease
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Person
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publication
Trinucleotide Repeat Expansions and Human Genetic Disease
1995 |
Central Library of Charles University, Second Faculty of Medicine
publication
Hypervariable intronic region in NCX1 is enriched in short insertion-deletion polymorphisms and showed association with cardiovascular traits
2010 |
First Faculty of Medicine
publication
Detection of two Alu insertions in the CFTR gene
2008 |
Second Faculty of Medicine
publication
Detailed molecular characterization of a novel IDS exonic mutation associated with multiple pseudoexon activation
2017 |
First Faculty of Medicine