1. Deletion (deficiency)
mutations due to lack of chromosomal segments, a portion of chromosome disappeared.
2. duplication
mutation because of excess chromosome segments, the presence of extra genetic material
3. translocation
mutations are being exchanged segment of chromosome to nonhomologous
4. inversion
mutations that occur because of changes in gene location due pilinnya chromosomes during meiosis, upside down from the previous arrangement
5. Isokromosom
chromosomal mutations that occur in the loss of one chromosome arm
6. Katenasi (ring formation)
both ends of the chromosome arms fuse to form a circle like a ring.
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