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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.
What else can I help you with?
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 chromosomal mutation results in alagille syndrome?
translocation
What are four-types of chromosomal mutations?
Four Types of Chromosomal Mutations include-Duplication-Translocation-Inversion-Deletion
What Happens during movement of chromosome to a non homologous chromosomes?
chromosomal Translocation
What is caused by chromosomal translocation?
Chromosomal translocation can lead to genetic disorders and cancer. It can result in the fusion of genes from different chromosomes, creating abnormal gene products that may interfere with normal cellular functions. This can disrupt gene expression and lead to the development of various health conditions.
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 is transfer of genes between nonhomologous chromosomes?
Transfer of genes between nonhomologous chromosomes is known as chromosomal translocation. It can result in the fusion of two chromosomes or the exchange of genetic material between them. This process can lead to genetic abnormalities and diseases.
4 types of mutation resulting from the breakage of chromosomes?
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.
The exchange of parts between non homologous chromosomes...?
is known as chromosomal translocation. This process can lead to genetic disorders if it disrupts the normal function of genes located on the chromosomes involved. Chromosomal translocations can be balanced, in which case they may have no noticeable effect, or unbalanced, which can result in various health issues.
How many different types of chromosomal abnormalities are there?
There are several types of chromosomal abnormalities, including deletion, duplication, inversion, translocation, and aneuploidy. These abnormalities can lead to genetic disorders and abnormalities in human development.
A mutation caused by a piece of DNA breaking away from its chromosome and becoming attached to a nonhomologous chromosome is called?
This type of mutation is called a translocation mutation. It involves the movement of a segment of DNA from one chromosome to another non-homologous chromosome, leading to potential genetic changes and abnormalities.
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.
