Inheritance, cystic fibrosis and genetic screening: exam questions

7 questions, 26 marks. Write your answers on paper, then open each mark scheme.

Question 1

Unit 1 style

Two people who both have blood group AB (genotype IᴬIᴮ) have a child. Which blood group could the child NOT have?

  1. Group A
  2. Group B
  3. Group AB
  4. Group O
[1 mark]
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Question 2

Unit 1 style

The table describes the members of one family in which some individuals have a genetic condition. Use the table to deduce whether the allele that causes the condition is dominant or recessive. Explain your answer.

Family with a genetic condition
IndividualSexConditionParents
I-1MaleNot affected—
I-2FemaleNot affected—
II-1FemaleAffectedI-1 and I-2
II-2MaleNot affectedI-1 and I-2
[4 marks]
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Question 3

Unit 1 style

Red-green colour blindness is caused by a recessive allele (Xᵇ) on the X chromosome. A man with normal colour vision and a woman who is a carrier of the allele plan to have a child. Draw a genetic diagram and give the probability that their first child is a colour-blind boy.

[3 marks]
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Question 4

Unit 1 style

Explain how a mutation in the gene for the CFTR protein leads to the symptoms of cystic fibrosis in the gaseous exchange system and the digestive system.

[5 marks]
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Question 5

Unit 1 style

Compare and contrast amniocentesis and chorionic villus sampling.

[4 marks]
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Question 6

Unit 1 style

A couple who are both carriers of the cystic fibrosis allele decide to have a child by IVF with pre-implantation genetic diagnosis (PGD). Describe how PGD is carried out.

[3 marks]
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Question 7

Unit 1 style

Discuss the ethical and social issues relating to prenatal genetic screening, from religious, moral and social viewpoints.

[6 marks]
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