This document summarizes key concepts about genes, chromosomes, DNA, and genetic inheritance. It discusses how genes are found on chromosomes and contain DNA, and how parents pass genes to offspring through sex cells like egg and sperm cells. The document also covers genetic disorders like cystic fibrosis and Huntington's disease, explaining how different genetic conditions can be dominant or recessive based on whether one or two copies of an allele are required to exhibit traits. Environmental factors that can influence traits are also mentioned.

4. Nucleus, chromosome and gene

19. Inheriting the Huntington's allele In this example, both parents carry one copy of the Huntington’s allele . Both have the disorder. There is a 3:4, or 75 per cent, chance of them producing a child with the disorder. Note that in an individual family, by chance, all of the children might inherit the disorder. It is also possible for none of them to inherit the disorder, although this is less likely than in the first example. In this instance, one parent, the mother, carries one copy of the Huntington’s allele. The father carries two copies. Both have the disorder. All of their children will have it, too.