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CCHS Biology Chapter 7

AB
allelean alternative form of a gene
codominancecondition in which both alleles for a gene are expressed when present
continuous variationa genetic pheonomenon in which a trait is controlled by several genes and therefore exhibits a variety of phenotypes
cross-pollinationtransfer of pollen from the male structures of one plant to the female structures of a different plant of the same species
dihybrid crossa cross that involves two pairs of contrasting traits
dominanttrait that is expressed when its allele is homozygous or heterozygous
F1 generationthe offspring from a cross of two varieties
F2 generationthe offspring from crosses among individuals of the F1 generation
genetic disorderharmful effect, such as sickle cell anemia, produced by mutated genes
geneticsstudy of heredity
genotypegenetic constitution of an organism as indicated by its set of alleles
hemoglobincomponent of red blood cells that binds with and carries oxygen through the body
hemophiliagenetic disorder that impairs the blood's ability to clot and can cause excessive bleeding
hereditytransmission of genetic traits from parent to offspring
heterozygousrefers to a pair of genes, or an individual, with two different alleles for a trait
homozygousrefers to a pair of genes, or an individual, with two identical alleles for a trait
incomplete dominancecondition in which a trait is intermediate between two parents
law of independent assortmentlaw stating that pairs of genes separate independently of one another in meiosis
law of segregationlaw stating that pairs of genes separate in meiosis and each gamete receives one gene of a pair
monohybrid crosscross involving one pair of contrasting traits
multiple alleleshaving more than two alleles (versions of the gene) for a genetic trait
mutationchange in the DNA of a gene or chromosome
pedigreefamily history of traitsrecorded over a generation
P generation(parental generation) plants that displayed one form of a particular trait
phenotypeobservable characteristic of a a trait
phenylketonuria (PKU)genetic disorder in which an individual lacks an enzyme that converts the amino acid phenylalanine into the amino acid tyrosine
probabilitythe likelihood that a specific event will occur
Punnett squarediagram used by biologists to predict the probable outcome of a cross
recessivethe trait that is not expressed in F1 generation after crossing
self-pollinationprocess by which a plant pollinates itself
sex-linked traita trait that is determined by a gene found on the x chromosome
sickle cell anemiacondition caused by amutant allele that produces a defective form of the protein hemoglobin
true-breedingdisplaying only one form of a particular trait in offspring


Mrs. Pyne

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