The extra X chromosome is received from mother.
<h3><u>Explanation</u>:</h3>
Klinefelter's syndrome is the condition of chromosomal aberration where the person has an extra X chromosome. This means the genotype of the person is 44+XXY and the total chromosome number is 47. This condition is achieved due to inappropriate meiotic division and one of the sperm or ovum has the an extra X chromosome.
Here both the parents are normal in terms of colour vision. So the father cannot have the gene of colour blindness because if it was present, then father would have been colour blind because he has only one X chromosome per cell. So its present in mother who is heterozygous in terms of colour blind gene. So the extra X chromosome also came from her which made the presence of two defective X chromosomes in the offspring and made it colour blind.
When the two waves meet, there are two possibilities:
1.If the waves were both in phase and moving in the same direction, then, the amplitude will double, this is called constructive interference.
2. If the two waves were exactly out of phase, then they will try to move the water surface in all directions, thus, no movement and the waves cancel out. This is called destructive interference.
Answer:
the correct answer is option b, as energy follow in such condition is uni directional
Answer:
A frameshift changes every codon past it. A base substitution only changes one codon.
Explanation:
DNA is comprised of nucleotides (A, C, T, G) that make up amino acids. Every three bases is called a codon and represents an amino acid.
In a frameshift mutation, a nucleotide is either added or deleted from the sequence. This offsets the entire sequence after it because the reading frame shifts. Here's an example:
ACTGCTATCGTCATC
If another T is added in between the first and second codons, then every codon after will be changed.
ACT>T<GCTATCGTCATC
A substitution mutation is usually less severe, as it only alters one codon in the sequence. These occur when one nucleotide is replaced by another one. Here's an example:
ACTGCTATCGTCATC
Let's say the first G is replaced by a T.
ACT>T<CTATCGTCATC
As you can see, none of the other codons changed.
Typically, a frameshift mutation is considered worse than a substitution mutation.
Answer:
d is the correct answer of your question
