F1 generation – children/offspring
Alleles – one member of a pair or series of genes that occupy a specific position on
a specific chromosome
Dominant allele – the allele, represented by a capital letter, that shows in the
phenotype
Recessive allele – the allele, represented by a lower case letter, that is hidden in the
phenotype
Law of segregation – the principle, originated by Gregor Mendel, stating that during
the production of gametes the two copies of each hereditary factor segregate so
that offspring acquire one factor from each parent
Punnett Square – a type of grid used to show the gametes of each parent and their
possible offspring
Homozygous – having identical pairs of genes for any given pair of hereditary
characteristics
Carriers - an individual that carries one gene for a particular recessive trait
Tay-sachs disease – a rare fatal hereditary disease, occurring chiefly in infants and
children, characterized by a red spot on the retina, gradual blindness, and paralysis
Sickle cell disease – A chronic, usually fatal anemia marked by sickle-shaped red
blood cells