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Polyploidy
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What type of mutation results in the Reversal of the direction of part of the chromosome?
The type of mutation that results in the reversal of the direction of part of the chromosome is called an inversion mutation. It occurs when a segment of the chromosome breaks and is reinserted in the opposite orientation. This can disrupt the normal functioning of genes located within the inverted region.
What is the term for any permanent change in a gene of chromosome?
The permanent change in a gene or a chromosome is called Mutation.
What type of mutation occurs when part of a chromosome is missing after replication?
Deletion
What is an mutation?
An Inversion mutation is a mutation that causes a reversal in the order of a segment of a chromosome within the chromosome, or a gene.
What gene or chromosome is mutated in the hemophilia disorder?
There are two types of hemophilia. Type A: A mutation in the factor VIII gene. Type B: A mutation in the IX gene.
Whats a change in gene or chromosome?
A change in a gene or chromosome is called a: Mutation
Where does the chromosome of galactosemia is located on?
Some scientists say: -The insulin dependent DDM1, Diabtese mellitus is on chromosome 6 -Type 1 Diabetes was found on chromosome 1q42, and possibly 11 -Type 2 Diabetes on Chromosomes 12 and/or 20
What type of mutation causes Edwards' syndrome?
An extra copy of Chromosome 18
What is the DNA chromosome called that breaks off and reattaches to a homologous chromosome that is paired up in meiosis?
This is a type of mutation called translocation.
What is a change or error in the structure of a gene or chromosome?
Chromosomal mutation
Mutation is any change in a gene or chromosome?
mutations
What are four of chromosomal mutation?
Four types of chromosomal mutations are Down syndrome (which is a mutation in which there are three copies of chromosome 21), Kinefelter Syndrome (which is a mutation in which a male has an extra X-chromosome), Turner Syndrome (which is a mutation in which a female is missing an X-chromosome), and Patau Syndrome (which is a mutation in which there are three copies of chromosome 13).
