A prospective groom, who is healthy, has a sister with cystic fibrosis (CF), an autosomal recessive disease. Their parents are normal. The brother plans to marry a woman who has no history of CF in her family. What is the probability that they will produce a CF child? They are both Caucasian, and the overall frequency of CF in the Caucasian population is 1/2500—that is, 1 affected child per 2500. (Assume the population meets the Hardy-Weinberg assumptions.)

Explanation:

From the given information:

Since the parent are normal; Let assume that their trait is Pp

The affected sister  will be recessive in nature, so the trait will be pp

Now, the husband who is the groom will be a carrier with a probability of 2/3 since her sister is affected.

Also, the wife will be carrying a heterozygous trait since she is normal as well.

However, using Hardy-Weinberg assumption:

q = 0.02

Recall that:

Thus,

2pq = 0.0392

Finally, the required probability that there will be an affected offspring amongst the family is:

succession returns a disturbed

ecosystem to a more stable state. this is also classified into two (2) types:

primary succession and secondary succession. the primary succession arises when

a new land is transformed and a bare rock has been exposed providing an environment

that can be occupied for the first time. while, secondary succession occurs

when a previously occupied environment was disturbed that kills much of all its

community

explanation: