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Liono4ka [1.6K]
3 years ago
12

When chromosomes do not separate you end up with a

Biology
1 answer:
dusya [7]3 years ago
7 0

Answer:

The phenomenon of unequal separation in meiosis is called nondisjunction. If nondisjunction causes a missing chromosome in a haploid gamete, the diploid zygote it forms with another gamete will contain only one copy of that chromosome from the other parent, a condition known as monosomy. I think sorry if wrong ;)

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The protein covering of a virus is called a capsid.

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Two factors which cause global climate change are listed below.
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Answer:

c. Factors 1 and 2 may be influenced by both nature and human factors

Explanation:

The sea level rising and the change in the atmospheric gases are both processes that are influenced by the nature, as well as by the human activities. Naturally, the earth has its own cycles, known as Milankovich cycles, through which the Earth warms up, or cools down, resulting in change of the atmospheric gases, and in accordance to that, change in the sea levels depending on the global climate. The humans to have become a big factor in the past few hundred years. The reason for that is that the humans with their activity started to release lot of greenhouse gases into the atmosphere, especially CO2 and methane. That has been changing the composition of the atmosphere, and the temperatures have been rising. The higher the temperatures, the more ice is melting around the poles and on the high mountains, resulting in an increase in the sea levels.

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3 years ago
Cystic fibrosis (CF) is one of most common recessive disorders among Caucasians it affects 1 in 1,700 newborns. What is the expe
Phantasy [73]

Answer: The expected frequency of carriers is P(Aa)=0.046.

The proportion of childs with CF is P(aa)=0.024.

25% of having a child with CF (aa).

Explanation:

Hardy-Weinberg's principle states that in a large enough population, in which mating occurs randomly and which is not subject to mutation, selection or migration, gene and genotype frequencies remain constant from one generation to the next one, once a state of equilibrium has been reached which in autosomal loci is reached after one generation. So, a population is said to be in balance when the alleles in polymorphic systems maintain their frequency in the population over generations.

Given the gene allele frequencies in the gene pool of a population, it is possible to calculate the expected frequencies of the progeny's genotypes and phenotypes. <u>If P = percentage of the allele A (dominant) and q = percentage of the allele a (recessive)</u>, the checkerboard method can be used to produce all possible random combinations of these gametes.

Note that p + q = 1, that is, the percentages of gametes A and a must equal 100% to include all gametes in the gene pool.

The genotypic frequencies added together should also equal 1 or 100%, and all the equations can be summarized as follows:

p+q=1\\(p+q)^{2}  = p^{2} +2pq+q^{2} = 1\\P(AA)=p^{2} \\P(aa)=q^{2} \\P(Aa)=2pq1

So, there are 1700 individuals and only one is affected. Since it is a recessive disorder, the genotype of that individual must be aa. So the genotypic frequency of aa is 1/1700=0.000588.

Then, P(aa)=q^{2}=0.000588. And with that we can calculate the value of q,

P(a)=q=\sqrt{0.000588}=0.024

And since we know that p+q=1, we can find out the value of p.

p+0.024=1\\1-0.024=p\\p=0.976

Next, we find out the genotypic frequency of the genotype AA:

P(A)=p=0.976\\P(AA)=p^{2} = 0.976^{2}=0.95

Now, we can find out the genotypic frequency of the genotype Aa:

P(Aa)=2pq=2 x 0.976 x 0.024 = 0.046

Notice than:

p^{2} + 2pq + q^{2} = 1\\x^{2} 0.976^{2} + 2 x 0.976 x 0.024 + 0.024^{2} = 1

Then, the expected frequency of carriers is P(Aa)=0.046

The proportion of childs with CF is P(aa)=0.024

If two parents are carriers, then their genotypes are Aa.

Gametes produced by them can only have one allele of the gene. So they can either produce A gametes, or a gametes.

In the punnett square, we can see that there genotypic ratio is 2:1:1 and the phenotypic ratio is 3:1. So, there is a probability of 25% of having an unaffected child, with both normal alleles (AA); 50% of having a carrier child (Aa) and 25% (0.25) of having a child with CF (aa).

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