Question

Suppose that you are studying is a rare recessive condition in humans whereby affected individuals are...

Suppose that you are studying is a rare recessive condition in humans whereby affected individuals are unable to metabolize a sugar found in certain foods. A woman and her husband are both heterozygous for the allele causing the condition.

A) If the woman is pregnant with twins and the twins are dizygotic (non-identical), what is the probability that both twins will be girls and be affected?

B) If the couple has four affected children, what is the probability that a fifth child will also be affected?

C) What is the probability if the girl twins are identical (monozygotic) and both are affected?

D) If the woman gives birth to four children, what is the probability that none of them will be affected?

E) If the couple has four children, what is the probability that one of will be affected?

F) If the couple has four children, what is the probability that the first two will be affected while the second two will be unaffected?

G) If the couple has three children, what is the probability that two will be affected while one will be unaffected, regardless of birth order?

Homework Answers

Answer #1

Solution:

It is a autosomal recessive disease. Ratio when 2 heterozygous are crossed is 1:2:1 in which three are normal and one is affected.

A) Probability of 1st twin to be a girl = 1/2.

Probability of 2nd twin to be a girl = 1/2

Probability of both the girls to be affected = 1/2×1/2×1/4=1/16

B).  Probability that fifth child is affected = 1/4

C). Probability of identical twins to be girls= 1/2.

Probability of both the identical twins to be affected= 1/2×1/4=1/8

D) .

Probability that none of them is affected

i.e all four of them are normal is= 3/4×3/4×3/4×3/4= 81/256

E). Probability that one child willbe affecd= (4!/3!×1! )× (3/4)³×(1/4)¹= 27/64

F) . Probability that first two are affected and second two are unaffected= 1/4×1/4×3/4×3/4 = 9/256

G). Probability that 2 will be affected and one will be Normal = (3!/2!×1!)×(3/4)×(1/4)²= 9/64

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
A woman (Tina) has a certain genetic condition (is affected). She goes to a genetic counselor...
A woman (Tina) has a certain genetic condition (is affected). She goes to a genetic counselor to learn about the inheritance pattern of the condition and to ascertain the chance that she might pass it to her offspring. The following is the information she gives the Genetic Counselor. (assume that this condition displays 100% penetrance, results from a single genetic mutation and exhibits complete dominance) 1) Tina is the fourth born of seven children. Her oldest sibling is an affected...
Seborrheic keratosis is a rare hereditary skin condition caused by an autosomal dominant mutation. Affected people...
Seborrheic keratosis is a rare hereditary skin condition caused by an autosomal dominant mutation. Affected people have skin marked with a number of small, sharply margined, yellowish or brownish areas covered with a thin, greasy scale. An affected man, whose father also had keratosis but whose mother did not, marries a normal woman and they have four children. A) What is the chance that all four are normal? B) What is the chance that at least two of the four...
Galactosemia is a recessive human disease that is treatable by restricting lactose and glucose in the...
Galactosemia is a recessive human disease that is treatable by restricting lactose and glucose in the diet. Susan Smithers and her husband are both heterozygous for the galactosemia gene. If the couple has four children with galactosemia, what is the probability that their next child will have galactosemia?
A woman has just had twins, a boy and a girl. The woman’s father has two...
A woman has just had twins, a boy and a girl. The woman’s father has two X-linked recessive disorders, haemophilia and colour-blindness, but the woman is unaffected. The father of the children has neither disorder. Both disorders are completely penetrant. The loci for the two traits are known to be 5cM apart. a) What is the probability that the boy will be colour-blind but not haemophilic? Explain your answer, including showing the genotypes and phenotypes of the family. [10 marks]...
A man with hemophilia (a recessive, sex-linked condition) and a woman that carries the hemophilia allele...
A man with hemophilia (a recessive, sex-linked condition) and a woman that carries the hemophilia allele have a daughter with normal phenotype. Define allele symbols for the hemophilia and normal alleles. Draw a pedigree and indicate the genotype of each individual in the pedigree. The daughter marries a man who is normal for the trait. What is the probability that a daughter of this pair will be a hemophiliac? What is the probability that a son will be a hemophiliac?...
A couple wishes to have exactly two female child in their family. Suppose that P(male birth)...
A couple wishes to have exactly two female child in their family. Suppose that P(male birth) = 0.4. They will have children until this condition is fulfilled. 1. What is the probability that the family has x male children? 2. What is the probability that the family has four children? 3. What is the probability that the family has at most four children? 4. How many male children would you expect this family to have? 5. What is SD of...
A couple wishes to have exactly two female child in their family. Suppose that P(male birth)...
A couple wishes to have exactly two female child in their family. Suppose that P(male birth) = 0.4. They will have children until this condition is fulfilled. Introduce a random variable X. b. (5 pts) What is the probability that the family has x male children? c. (5 pts) What is the probability that the family has four children? d. (5 pts) What is the probability that the family has at most four children? e. (5 pts) How many male...
Sex-linked crosses 4. Hemophilia is an X-linked disease, meaning that the gene that causes the disease...
Sex-linked crosses 4. Hemophilia is an X-linked disease, meaning that the gene that causes the disease is found on the X chromosome. Affected males only have to have one allele to have the disease (XhY), while affected females have to have two alleles (XhXh). Imagine that an affected male has children with an unaffected carrier female. a. What are the genotypes of the parents in this cross? b. Draw a Punnett cross to show the offspring of this couple. c....
An obstetrician asked for a bioethics consultation to consider the request of Charles and Amanda Harrleson...
An obstetrician asked for a bioethics consultation to consider the request of Charles and Amanda Harrleson for genetic testing and possible elective abortion. Mrs. Harrelson, who was pregnant for the first time, was three months into an apparently normal pregnancy. She and her husband were both achondroplastic dwarfs. They seemingly were financial comfortable and well-adjusted to their physician conditions. They requested testing of their developing fetus for the evidence of achondroplasia. The condition results from a mutation of a single...
Please show all work step by step. Thank you. 1) The skin of the bright orange...
Please show all work step by step. Thank you. 1) The skin of the bright orange South American toad secretes a lethal neurotoxin. Assume that the toxin is produced by an enzyme encoded by a gene that has two alleles: T (dominant, wild-type enzyme/toxin) and t (recessive, no enzyme/toxin produced). The neurotoxin is secreted by means of a protein S produced by the wild-type gene S. The recessive allele s does not produce protein S (thus no secretion of the...
ADVERTISEMENT
Need Online Homework Help?

Get Answers For Free
Most questions answered within 1 hours.

Ask a Question
ADVERTISEMENT