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: core
Explanation:
The core is the thickest layer of the Earth, and the crust is relatively thin, compared to the other layers.
A DNA molecule consists of two strands of nucleotides twisted together to form a double helix. The sugar-phosphate backbone is found on the outside of this helix and the bases are found braching towards the middle. Hydrogen bonds join the thenitrogenous bases and hold the two strands together.
Therefore your answer is sugar and phosphate.
Answer:
The different possible genotypes are AA, AO, BB, BO, AB, and OO. These are derived according to the A, B and O blood group model.
The table is given below:
Blood Type Genotype
Blood Type A Genotypes AA or AO
Blood Type B Genotypes BB or BO
Blood Type AB Genotype AB
Blood Type O Genotype OO
The alleles A and B exhibit a greater dominance than O. This is the reason why the Parent of Blood type A will form the Genotype AO.
