The answer is 23.
A human being receives 23 chromosomes from each parent. So each human has 46 chromosomes. Chromosomes X and Y determines your sex.
Answer:
1 . The stage on the first meiotic division when the homologous chromosomes move to opposite poles but the sister chromatids remain together
: b. Anaphase I
2 . The stage in the second meiotic division where sister chromatids migrate to opposite poles
: c. Anaphase II
3 . A structure on the chromosome that holds a pair of chromatids together during replication
: f. centromere
4 . A double-stranded chromosome following replication attached by a centromere
: d. chromatid
5 . A condition where non-sister chromatid of homologous chromosomes exchange genes
: e. crossing over
6 . The stage in the first meiotic division where the homologous chromosomes line up as a pair
: a. Metaphase I
7 . The stage in the second meiotic division where the chromatid pair lines up at the equator of the cell: g. Metaphase II
Explanation:
DNA replication occurs during the S phase of the interphase of the cell cycle. The replicated DNA molecules are accommodated in two sister chromatids of a chromosome that are held together by a centromere.
During prophase I, the chromatids of a homologous chromosome pair exchange a genetic segment. This process is called crossing over. It generates recombinant chromatids with new combinations of genes.
Metaphase I of meiosis I includes the alignment of homologous pairs of chromosomes at the cell's equator. This is followed by separation and movement of homologous chromosomes to the opposite poles of the cell during anaphase I.
Metaphase II of meiosis II includes the alignment of individual chromosomes, each with two sister chromatids, on the cell's equator. During anaphase II, splitting centromere separates the sister chromatids which then move to the opposite poles of the cell.
Answer:
Brain
Explanation:
The brain has nerve endings that responds to stimulations such as sensory stimulations
Answer:
50% or 1/2. The result remains unchanged if the husband were to have G6PD.
Explanation:
For X-linked recessive inheritance, a female (XX) needs two recessive alleles to be affected while a male needs only one (XY). It is hypothetically assumed that the Y chromosome does not carry any trait.
Assuming the allele for the disease is represented by g, a woman whose father suffered from G6PD is a carrier for the disease with genotype 
. A normal man will have the genotype 
. When the 2 marries:
x = 
It thus means that 50% or 1/2 of their sons will be expected to have G6PD.
Now, assuming the husband has G6PD, the mating becomes:
x 
= 
50% or 1/2 of their sons is still expected to have G6PD. The ratio remains unchanged.
