A human gene carries a certain disease from a mother to her child with a probability rate of 0.54. That is, there is a 54% chance that the child becomes infected with the disease. Suppose a female carrier of the gene has five children. Assume that the infections, or lack thereof, are independent of one another. Find the probability that all five of the children get the disease from their mother. Question 16 options: 0.024 0.954 0.046 0.021
Given : n=5 , p=0.54 , q=1-p=0.46
Here ,
The pmf of X is ,
; x=0,1,2,..........,n
=0 ; otherwise
Therefore ,
Hence , the probability that all five of the children get the disease from their mother is 0.046.
A human gene carries a certain disease from a mother to her child with a probability...
3) A human gene carries a certain disease from the mother to the child with a probability rate of 30%. That is, there is a 30% chance that the child becomes infected with the disease. Suppose a female carrier of the gene has five children. Assume that the infections of the five children are independent of one another. Find the probability that at least one of the children get the disease from their mother.
A human gene carries a certain disease from the mother to the child with a probability rate of 47%. That is, there is a 47% chance that the child becomes infected with the disease. Suppose a female carrier of the gene has three children. Assume that the infections of the three children are independent of one another. Find the probability that all three of the children get the disease from their mother. 0.132 0.896 0.104 0.149
A certain disease can be passed from a mother to her children. Given that the mother has the disease her children independently will have it with probability 1/2. Given that she doesn't have the disease, her children won't have it either. A certain mother, who has probability 1/3 of having the disease, has two children. (1) Find the probability that neither child has the disease. (2) Is whether the older child has the disease independent of whether the younger child...
Mendelian Genetics The gene involved in the disease Sickle Cell Anemia (SCA) is on human chromosome 11. Allele “A” is the normal form of the gene and codes for a part of the protein complex called hemoglobin. Hemoglobin is required for your blood cells to carry oxygen. Allele “a” is an abnormal form of the gene. The hemoglobin protein made from the “a” allele is defective. Red blood cells containing the defective protein are very fragile. This disease is recessive–meaning...
question 5-52 93 Dd D) dd D) aa x aa C) human height E) DI 4.Which of these crosses will only produce heterozygous offspring? B) AA x Aa C) Aa x Aa E) Aa x aa 5. Which of the following human traits is an example of codominance? A) sickle-cell anemia D) AB blood type B) variation in eye color 6. Which of the following is true regarding an individual who has inherited one sickle-cell gene and one normal gene...