If both, Jenifer and Bill are the
carriers (have one allele for the achondroplasia) that theirs genotypes are Aa (A is dominant, a is recessive allele). In this case:
P: Aa x Aa
F: AA Aa Aa aa
This means that ΒΌ (25%) is the possibility for child to have achondroplasia.
Second case is if one of the parents have homozygous recessive genotype aa (not having allele for achondroplasia):
P1: Aa x aa
F: Aa Aa aa aa
This means that none of the child will inherit both alleles.