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during meiosis
It is caused by a gene mutation in the single gene on chromosome 7 that produces a protein known as CFTR.
A translocation chromosomal mutation will result when two non-homologous chromosomes each broken by some sort of clastogen and then are swapped.
You can have a baby with physical/mental deformities or death of the child.
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 gene is passed on from generations and a chromosome is just found in certain cells
chromosomal mutation
Chromosomal mutation
A chromosomal mutation can occur for a variety of reasons. Some people think that DownÕs syndrome is a mutation but it is more an additional chromosome than a mutation.
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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