How is nominal scale type related to diversity?

Each of the four pedigrees that follow represents a human family within which a genetic disease is segregating. Affected individ

Ne4ueva [31]

Answer:

The following four traits are -:

Pedigree 1 - A recessive trait (autosomal recessive) is expressed by pedigree 1.
Pedigree 2- Recessive inheritance is defined by Pedigree 2.
Pedigree 3 - The inheritance of the dominant trait (autosomal dominant) is illustrated by Pedigree 3.
Pedigree 4- An X-like dominant trait is expressed by Pedigree 4.

Explanation:

Explaination of each pedigree chart-

Pedigree 1 demonstrates the recessive trait since their children have been affected by two unaffected individuals. If the characteristics were X-linked, in order to have an affected daughter, I-1 would have to be affected. $X^A$ In this, both parents are autosomal recessive trait carriers, so the child will be affected by a 1/4 (aa)
Recessive inheritance is defined by Pedigree 2. This is X-related inheritance as autosomal recessive inheritance has already been accounted for in part 1. This inference is confirmed by evidence showing that the father (I-1) is unaffected and that only the sons exhibit the characteristic in generation II, suggesting that the mother must be the carrier. The individual I-2 is a carrier for this X-linked trait. A typical Xa chromosome is attached to the unaffected father (I-1), so the chance of carrier II-5 is 1/2. Probability of an affected son = 1/2 (probability II-5 is a carrier) x 1/2 (probability II -5 contributes ( $X^A$ ) x 1/2 (probability of Y from father II-6) = 1/8. An affected daughter's likelihood is 0 because a typical $X^A$ must be contributed by II-6.
The inheritance of the dominant trait is demonstrated by Pedigree 3 because affected children still have affected parents (remember that all four diseases are rare). The trait must be autosomal dominant because it is passed down to the son by the affected father. There is a 1/2 risk that the heterozygous mother (II-5) would pass on mutant alleles to a child of either sex for an autosomal dominant feature.
Pedigree 4 is an X-linked dominant function characterized by the transmission to all of his daughters from the affected father but none of his son. On the mutant X chromosome, the father (I-1) passes on to all his daughters and none of his sons. As seen by his normal phenotype, II-6 therefore does not bear the mutation. An affected child's likelihood is 0.

In the question the pedigree chart was missing ,hence it is given below.

7 0

3 years ago

What is the colorless, odorless gas that binds to red blood cells causing the body not to get the oxygen it needs?

Juliette [100K]

Answer:

Therefore,when carbon monoxide is present,it blind to hemoglobin preferentially over oxygn.As a result,oxygen cannot blind to hemoglobin ,so very little oxygen is transported through the body carbon monoxide is a colorless odorless gas and is therefore difficult detect.

7 0

2 years ago

Why are dead or weakened viruses used instead of normal viruses to create a vaccine?

vodomira [7]

I think its because vaccines are just to help your body learn how to fight off the virus, it’s not to actually give you the virus. Hope this helped!

5 0

2 years ago

Read 2 more answers

How could you investigate the idea that DNA is found only in living or once-living things?

Phoenix [80]

Answer: Cloning, dude just watch jurassic park

Explanation:

4 0

3 years ago

Why do you think that there are earthquakes in mid-america where there are no fault lines

Dvinal [7]

Earthquakes only occur at transfer boundaries where two tectonic plates will slide or rub past each other.
If there are no boundaries in mid-America, then earthquakes are not possible.

5 0

3 years ago