Answer: The mother of the man can be either XHXH or XHXh and pass her normal allele to the son and his father can be either XHY or XhY, he only passes his Y chromosome. The mother of the woman can be XHXH or XHXh and the father could be XhY, then she could have inherited the normal allele from the mother and the affected allele from the father. But also, the mother of the woman could be XHXh or XhXh and the father could be XHY, so in this case she could have inherited the normal alele from the father and the affected allele from the mother.
Explanation:
Hemophilia is an inherited bleeding disorder in which the blood does not clot properly. This can cause bleeding either spontaneously or after an injury.
<u>It is related to the X chromosome and it is recessive for females</u>, this mean they need both affected alleles to develop the trait. <u>Males only need one recessive allele because they only have one X chromosome</u>. This means that females need both parents to be at least carriers (although one or both can also have the disease or both recessive alleles). While males inherit it only from the mother, either she is a carrier (one recessive allele) or she has the disease (both recessive alleles). Then the mother passes the X chromosome with the affected allele to the son, and that son only receives the Y chromosome from the father, which does not have the gene that determines this disease.
If the mother is a carrier, her genotype is XHXh, being XH the normal allele and Xh the affected allele. She does not have hemophilia because she has a dominant allele. The father is XHY, so he does not have the disease because his only allele is normal (dominant)
The mother of the man can be either XHXH (she can only pass a normal allele) or XHXh and pass her normal allele to the son (in this case, the recessive allele is not inherited by chance.) His father can be either XHY or XhY, he only passes his Y chromosome which is not related to the disease. The mother of the woman can be XHXH or XHXh and the father could be XhY, then she could have inherited the normal allele from the mother and the affected allele from the father. But also, the mother of the woman could be XHXh or XhXh and the father could be XHY, so in this case she could have inherited the normal alele from the father and the affected allele from the mother.
Answer: In females, most of gametogenesis occurs during embryonic development. Primordial germ cells migrate into the ovaries at week 4 of development and differentiate into oogonia (46,2N).
Explanation:
Answer:
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Explanation:
In evolutionary theory, adaptation is the biological mechanism by which organisms adjust to new environments or to changes in their current environment. ... The idea of natural selection is that traits that can be passed down allow organisms to adapt to the environment better than other organisms of the same species.
Multiply 5730 years by 2 since two half-lives have gone by for carbon.
<u>Explanation</u>:
The half-life of a radioactive isotope depicts the measure of time that it takes half of the isotope in an example decay. On account of radiocarbon dating, the half-existence of carbon 14 is 5,730 years
The half-life of carbon-14 is 5730 years.
In this manner, after
1 half-life there is 50 % = 1/2 of the first amount left.
2 half-lives there is 25 % = 1/4 of the first amount left.
25% is two half-lives.
Every 50% of life requires 5730 years.
So two half-lives require 2 × 5730
Which one do you want answered
