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What is trisomy mutation?
A trisomy is when a person has 3 versions of a chromosome. 'Normal' humans will only have 2 of each chromosome. For example, having 3 versions of chromosome 21 is known as Trisomy 21 or Down Syndrome.
Any permanent change in gene or chromosome of a cell?
A mutation is a permanent change in the gene or chromosome of a cell that can result in altered characteristics or function. Mutations can arise spontaneously during cell division or in response to external factors such as radiation or chemicals. These changes can be inherited or occur randomly in somatic cells.
Why does a detetion mutation usually cause more defect during protein synthesis than point mutation?
Mutation usually causes the entire base sequence to defect. This usually happens during the protein synthesis.
What mutation cause changes in the number of chromosome?
Aneuploidy mutation causes a change in the number of chromosomes. Aneuploidy occurs during cell division when the chromosomes do not separate properly resulting in a change in the number of chromosomes.
What Happens during movement of chromosome to a non homologous chromosomes?
chromosomal Translocation
What is the term for any permanent change in a gene of chromosome?
A mutation is the term for any permanent change in a gene or chromosome. Mutations can be caused by various factors, such as errors during DNA replication or exposure to certain environmental factors like radiation or chemicals.
What happens to the chromosome during the anaphase?
what happens to chromosomes during anaphase
Does mutation occur in klinefelter syndrome?
Mutation of a gene is not necessary for Klinefelter's Syndrome. It is an autosomal disorder meaning that an entire chromosome failed to disjunction during anaphase and so there are 2 X chromosomes and a Y chromosome.
Which types of mutation can be add genes to a chromosome?
Gene duplication is a type of mutation that can add genes to a chromosome. During gene duplication, a segment of DNA is copied and inserted into the chromosome, leading to an increase in the number of copies of a particular gene. This can result in gene families with multiple copies of a gene that may evolve new functions over time.
What is trisomy mutation?
A trisomy is when a person has 3 versions of a chromosome. 'Normal' humans will only have 2 of each chromosome. For example, having 3 versions of chromosome 21 is known as Trisomy 21 or Down Syndrome.
True or false a point mutation is the failure of a chromosome pair to separate during mitosis?
False. A point mutation is a change in a single nucleotide of DNA, leading to a change in the protein encoded by that gene. The failure of a chromosome pair to separate during mitosis is known as nondisjunction, which can lead to chromosomal abnormalities in the daughter cells.
Any permanent change in gene or chromosome of a cell?
A mutation is a permanent change in the gene or chromosome of a cell that can result in altered characteristics or function. Mutations can arise spontaneously during cell division or in response to external factors such as radiation or chemicals. These changes can be inherited or occur randomly in somatic cells.
How do you increase y chromosome?
This is not something you can choose to do. Sometimes a little accident happens during conception or during production of the sperm cell.
Why does a detetion mutation usually cause more defect during protein synthesis than point mutation?
Mutation usually causes the entire base sequence to defect. This usually happens during the protein synthesis.
What mutation cause changes in the number of chromosome?
Aneuploidy mutation causes a change in the number of chromosomes. Aneuploidy occurs during cell division when the chromosomes do not separate properly resulting in a change in the number of chromosomes.
What Happens during movement of chromosome to a non homologous chromosomes?
chromosomal Translocation
What happens during meiosis that results in a defect characterized by the deletion of a chromosome?
what happens during meiosis that results in a defect characterized by the deletion of chromosomes
