Standard layout for full marks

Examiners expect a consistent, clearly laid out genetic diagram. The recommended sequence is:

1. Parental phenotypes (state what each parent looks like).
2. Parental genotypes (use correct letter notation).
3. Gametes (circle them to show they are separate from genotypes).
4. Punnett square (one parent's gametes across the top, the other down the side).
5. Offspring genotypes and phenotypes.
6. Ratio (phenotype ratio, and genotype ratio if asked).

Missing the gametes line is the single most common reason for losing marks in genetics questions.

Understanding ratios and probability

The ratios from genetic diagrams are predicted or expected ratios based on probability. They do not guarantee the exact outcome.

Cross typeExpected phenotype ratio
Heterozygous x Heterozygous (Bb x Bb)3 dominant: 1 recessive
Heterozygous x Homozygous recessive (Bb x bb)1 dominant: 1 recessive
Co-dominance heterozygous x heterozygous1: 2: 1 (three phenotypes)
Sex determination (XX x XY)1 female: 1 male

With small numbers of offspring, actual results may differ from predicted ratios. The prediction becomes more accurate with larger sample sizes.

Why actual results differ from predicted ratios

Fertilisation involves random events. Each gamete combination is independent, like flipping a coin. Getting heads three times in a row does not change the probability of the next flip being heads. Similarly, having three offspring with the dominant phenotype does not make the next one more likely to show the recessive phenotype.

When exam questions ask why results differ from a 3:1 ratio, the answer is that fertilisation is random and small sample sizes produce results that may deviate from the predicted ratio by chance. Never say the cross "went wrong" or the ratio is "incorrect".