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Erstellt von gina_evans0312
vor mehr als 10 Jahre
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Activating Mutation
Deactivating mutation
Nucleotide substitution
Nucleotide substitution in Hereditary Haemachromatosis
Synonymous Mutation
Missense Mutation
Nonsense mutation
Nucleotide deletions/insertions
Splicing Mutations
Copy Number Variation
Genomic Disorders
DiGeorge Syndrome
CNV Occurence
Gene disruption
Gene fusion
Revealing positional effects