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  • 1. Mutations
  • 2. Substitution Mutation
    • Sickle cell anemia is due to a change in a single amino acid in the protein haemoglobin.
  • 3. Chromosomal Deletion
    • Cri-du-chat disorder occurs due to a deletion of part of chromosome 5.
  • 4. Duplication Mutation
    • Fragile X syndrome is a result of a short DNA sequence which is repeated 29 – 700 times.
  • 5. Inversion Mutation
  • 6. Translocation Mutation