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What is caused by chromosomal translocation?
A translocation chromosomal mutation will result when two non-homologous chromosomes each broken by some sort of clastogen and then are swapped.
What Happens during movement of chromosome to a non homologous chromosomes?
chromosomal Translocation
What change in the chromosomal structure involves the transfer of one section of a chromosome to a non homologous chromosome?
The change in chromosomal structure involving the transfer of one section of a chromosome to a non-homologous chromosome is known as a chromosomal translocation. This can result in genes being positioned in a different order or location, which can potentially disrupt gene function or regulation. Translocations are associated with various genetic disorders and can have significant effects on an individual's health and development.
Is DSRCT hereditary?
Based on our current knowledge of DSRCT, the answer is no. DSRCT, as we know it, occurs as a result of a chromosomal translocation (fusion of two different chromosomes) which happens somatically (after much of the development has completed).
What is the cause of chromosomal?
Chromosomal disorders are caused by abnormalities in the chromosomes.
Is translocation a type of mutation?
chromosomal mutation
What is caused by chromosomal translocation?
A translocation chromosomal mutation will result when two non-homologous chromosomes each broken by some sort of clastogen and then are swapped.
What chromosomal mutation results in alagille syndrome?
translocation
What are four-types of chromosomal mutations?
Four Types of Chromosomal Mutations include-Duplication-Translocation-Inversion-Deletion
Which chromosomal mutation results in Alagille syndrome?
Translocation. On Chromosome 20.
What Happens during movement of chromosome to a non homologous chromosomes?
chromosomal Translocation
What are the four types of chromosomal mutations?
There are four different types of chromosomal mutations: Deletions, Translocations, Duplications and Inversions
A mutation caused by a piece of DNA breaking away from its chromosome and becoming attached to a nonhomologous chromosome is called?
This condition is referred to as chromosomal translocation.
If a piece of DNA breaks off a chromosome and attaches itself to a nonhomologous chromosome at another location what type of change has occured?
If a piece of DNA breaks off a chromosome and attaches itself to a nonhomologous chromosome at another location translocation is the type of change that has occurred. The chromosomal pieces are moved to a new location.
What change in the chromosomal structure involves the transfer of one section of a chromosome to a non homologous chromosome?
The change in chromosomal structure involving the transfer of one section of a chromosome to a non-homologous chromosome is known as a chromosomal translocation. This can result in genes being positioned in a different order or location, which can potentially disrupt gene function or regulation. Translocations are associated with various genetic disorders and can have significant effects on an individual's health and development.
Is DSRCT hereditary?
Based on our current knowledge of DSRCT, the answer is no. DSRCT, as we know it, occurs as a result of a chromosomal translocation (fusion of two different chromosomes) which happens somatically (after much of the development has completed).
What are three types of chromosomal mutations?
Insertion, Deletion and Frameshift mutation. These are the 3 basic types of mutation, however, there are other types of mutations: substitution, translocation, duplication, inversion, transversion and transition.
