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this is possible. By all means yes. For the human DNA consists of 25 Chromosomes, but the string ends at 24. If by any means the 25th one is activated via science, humans will be like super humans. but there is a problem, you will age slower and even live 150 years longer. so yes, it can be done.
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∙ 15y ago
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What are examples of diseases caused by chromosomal mutation?
Down's Syndrome Kleinfelter's Syndrome
What are 4 types of chromosome structural changes?
The four types of alterations of chromosome structure are deletion, duplication, inversion, and reciprocal translocation. Deletion is the loss of one or more nucleotides from a gene by mutation; the loss of a fragment of a chromosome. Duplication is repition of a part of a chromosome resulting from fusion with a fragment froma homologous chromosome. Duplication can result from an error in meiosis or from mutagenesis. Inversion is a change in a chromosomeresulting from reattachment of a chromosome fragment to the original chromosome, but in a reverse direction. Mutagens and errors during mesosis can cause inversions. Translocation is the attachment of a chromosomal fragment to a nonhomologous chromosome.
What is the difference between translocation and nondisjunction?
Nondisjunction is when a Chromosome is unable to separate correctly during cell devision. Translocation (In Chromosomes) is when an abnormality is caused by the rearrangement of parts between non-homologous Chromosomes.
Can you still have a baby with a robertsonian translocation?
Yes, you can have a baby, even if you have a Robertsonian Translocation. (I have a Robertsonian Translocation and I have a three-year-old daughter.) There is a lot of genetic information involved, however, so the best thing to do would be to contact a genetic counselor who could advise you and explain your chances. For instance, a baby that survives to birth may have completely normal chromosomes or may also have a Robersonian Translocation, but in either of those cases, the baby would be fine. The good news, though, is that you can have a baby!
The genetic code is carried by the molecule in most organisms. chromosomal DNA guanine hereditary?
The genetic code is carried by the molecule in most organisms. chromosomal DNA guanine hereditary?
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 is the product of 16 and p?
16p
