tt
during meiosis
Trisomy 13, also known as Patau syndrome, is a chromosomal mutation where there is an extra copy of chromosome 13 in each cell. This condition can lead to various physical and intellectual disabilities.
You can have a baby with physical/mental deformities or death of the child.
Deletion: loss of a chromosomal segment. Duplication: repetition of a chromosomal segment. Inversion: reversal of a chromosomal segment. Translocation: movement of a chromosomal segment to a new location on a different chromosome.
There are many thousands of different mutations.
Chromosomal mutation can have lasting impacts on the person who this happens to. A version of a chromosomal mutation is the mutation that leads to Down's Syndrome.
A deletion, inversion, or translocation of a chromosome would be considered chromosomal mutations. These alterations involve changes in the structure or number of chromosomes, leading to genetic variations and potential health consequences.
chromosomal mutation
a gene is passed on from generations and a chromosome is just found in certain cells
gene mutation, chromosomal abberations
During meiosis
during meiosis
Nope, what you're thinking of is actually called an inversion mutation (a type of structural aberration); a chromosomal mutation is simply any sort of mutation that affects an organism's genotype.
Yes
Chromosomal mutation
translocation
during meiosis