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Inheritance: genetic crosses, sex and inherited disorders: GCSE Combined Science Biology practice questions

Foundation and Higher · Grade 6

A second set of questions on inheritance: genetic crosses, sex and inherited disorders. They are different from the ones on the topic page. Try each, then open the answer and compare your working.

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Question 1 Medium

Give the percentage chance of a baby being a girl.

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Answer: 50%

  1. Half the sperm carry X.
  2. So 50% are girls.

Question 2 Medium

A person has the genotype Ff for a recessive disorder. What word describes this person?

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Answer: carrier

  1. They have one copy of the allele.
  2. They are a carrier.

Question 3 Medium

Cystic fibrosis is caused by the recessive allele f. What is the genotype of a person who has cystic fibrosis?

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Answer: ff

  1. A recessive disorder needs two copies.
  2. So the genotype is ff.

Question 4 Medium

Two Bb parents have a child. What is the chance that the child shows the dominant feature? Give a percentage.

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Answer: 75%

  1. The boxes are BB, Bb, Bb and bb.
  2. Three out of four show the dominant feature, which is 75%.

Question 5 Hard

Give the ratio of dominant to recessive offspring from the cross Bb × bb.

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Answer: 1:1

  1. Two are Bb and two are bb.
  2. The ratio is 1 : 1.

Question 6 Hard

Two carriers of cystic fibrosis (Ff) have a child. What is the chance the child is a carrier? Give a percentage.

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Answer: 50%

  1. Two boxes in four are Ff.
  2. So the chance is 50%.

Question 7 Hard

A parent has genotype BB and the other has bb. What is the genotype of all the offspring?

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Answer: Bb

  1. Each gamete from BB carries B.
  2. Each gamete from bb carries b, so all are Bb.

Question 8 Hard

Polydactyly is caused by a dominant allele (P). One parent is Pp and the other is pp. What percentage of children are expected to have polydactyly?

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Answer: 50%

  1. The cross Pp × pp gives Pp, Pp, pp, pp.
  2. Half have polydactyly.

Question 9 Hard

Two parents without a condition have a child who has it. Is the condition dominant or recessive?

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Answer: recessive

  1. The parents must carry a hidden allele.
  2. So the condition is recessive.

Quick checks

Short questions with options. Choose one before you open the answer.

Check 1

What is an allele?

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A different version of a gene.

Check 2

What is a genotype?

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The combination of alleles a person has.

Check 3

What is a phenotype?

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The characteristic that shows from the genotype and environment.

Check 4

What is a dominant allele?

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An allele that shows even if there is only one copy.

Check 5

What is a recessive allele?

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An allele that only shows if two copies are present.

Check 6

What does homozygous mean?

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Having two identical alleles for a gene.

Check 7

What does heterozygous mean?

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Having two different alleles for a gene.

Check 8

What is the ratio from Bb × Bb?

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3 dominant to 1 recessive.

Check 9

What is the ratio from Bb × bb?

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1 dominant to 1 recessive.

Check 10

What are the sex chromosomes of a human female?

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XX.

Check 11

What are the sex chromosomes of a human male?

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XY.

Check 12

What is the chance of a baby being a boy?

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50%.

Check 13

What is polydactyly?

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Having extra fingers or toes, caused by a dominant allele.

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What is cystic fibrosis?

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An inherited disorder that causes thick, sticky mucus, caused by a recessive allele.

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What is a carrier?

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A person who has one copy of a recessive allele and does not show the disorder.

Check 16

What is embryo screening?

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Testing embryos for genetic disorders before they are placed in the womb.

Check 17

What is a gene?

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A section of DNA that codes for a protein.

Check 18

How many alleles of a gene does a body cell have?

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Two, one from each parent.

Check 19

How many alleles of a gene does a gamete have?

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One.

Check 20

What is a gamete?

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A sex cell, such as an egg or a sperm.

Check 21

Which sex chromosome do all eggs carry?

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X.

Check 22

What does a Punnett square show?

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The possible offspring from a genetic cross.

Check 23

Do two carriers always have a child with cystic fibrosis?

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No. Each child has a 25% chance.

Check 24

Name one concern about embryo screening.

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Embryos are destroyed, or it may lead to designer babies.

Check 25

Which parent decides the sex of a baby?

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The father, because the sperm carries X or Y.

Check 26

Can a small family differ from the 3 : 1 ratio?

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Yes. Each fertilisation is a chance event.

Check 27

What does a pedigree (family tree) show?

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How an inherited condition passes through a family.

Check 28

Two parents without a condition have an affected child. What does this show?

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The condition is recessive and both parents are carriers.

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