Answer;
-23 in males
In humans, 23 in males is the only homologous chromosome pair that isn't the same.
Explanation;
-In humans, each cell normally contains 23 pairs of chromosomes, for a total of 46.
-Twenty-two of these pairs, called autosomes, look the same in both males and females. The 23rd pair, the sex chromosomes, differ between males and females. Females have two copies of the X chromosome, while males have one X and one Y chromosome.
-The 22 autosomes are numbered by size. The other two chromosomes, X and Y, are the sex chromosomes.
Chromosomes! They contain the recipe for making a living thing. They are found in almost every cell's nucleus and are made from strands of deoxyribonucleic adic (DNA)
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.
The mechanisms by which restrictive lung diseases reduce lung function is increasing shortness of breath, chronic cough, weight loss, and fatigue.
<h3>How does the breathing process work?</h3>
Pulmonary ventilation consists of the flow of air into and out of the lungs with each cycle, which is composed of inspiration and expiration; it is a what they run on is the process of running the resources.
The respiratory pattern of individuals with restrictive diseases is a higher respiratory rate and lower tidal volume. of the airways, that is, they have a smaller radius. The faster the flow, the greater the friction of the molecules with the airways, further increasing the resistance.
See more about restrictive lung diseases at brainly.com/question/13047253
#SPJ1
