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Unit 6 Stack

QuestionAnswer
A complete haploid set of chromosomes of an organism. Genome
Reproduction in which organisms develop from unfertilized ova. Parthenogenesis
A chromosomal change that involves the addition or loss of entire genomes. Euploidy
Any cell or organism that has multiple genomes. Polyploid
Consists of three complete sets of chromosomes (genomes). Triploid
A poison that disrupts the spindle fiber during cell dicision, resulting in polyploid cells. Colchicine
Hacing four complete sets of chromosomes (genomes). Tetraploid
An organism in which the chromosome number is not an exact multiple of the haploid number. Aneuploid
The failure of a pair of homologous chromosomes to separate during meiosis. Nondisjunction
An abnormal condition in which there are three chromosomes in a set instead of two. Trisomy
A condition in which there is only one of a homologous chromosome pair. Monosomy
A genetic disorder caused by a trisomy of the twenty-first chromosome. Down Syndrome (trisomy 21)
A random change in a DNA molecule. Mutation
Mutation that causes the death of the organism. Lethal Mutation
The transfer of a chromosome segment to a nonhomologous chromosome; the movement of dissolved carbohydrates in plants. Translocation
Mutation involving the loss of a segment of chromosome during replication; a mutation involving the loss of a nucleotide from a DNA chain. Deletion
Chromosomal mutation in which genes break off a section of DNA and reattach but in the opposite order. Inversion
A changing of the gene itself, which alters the sequence of nucleotide bases within a gene. Gene Mutation
DNA mutation in which a nucleotide or nucleotides (other than three in number) are added to or taken from the chain so that subsequent codons are read incorrectly. Frame Shift
The formation of living organisms from nonliving materials. Spontaneous Mutation
A substance that induces mutation. Mutagen
A mutation that affects only body cells (not gametes). Somatic Mutation
A mutation that affects the gamete-producing cells. Germ Mutation
A mechanism that prevents badly deformed or genetically defective persons from living and/or reproducing. Genetic Screen
All the members of the same type of living things within an area. Population
The sum of all of the alleles that every member of a species' population could possess at a given time. Gene Pool
The differences between dfferent individual organisms of the sime kind; differences based on genotype; the expression of different individual characteristics in organisms of the same kind. Variation
The method for selecting breeding stock in which only the desirable organisms are selected. Mass Selection
The crossbreeding of two genetically unrelated individuals. Hybridization
An increased capacity for growth or strength in a hybrid. Heterosis
The mating of closely related organisms. Inbreeding
An organism that is homozygous for certain traits. Pure Strain
The science that deals with improvement of the uman race by applying principles of genetics. Eugenics
Medical and nonmedical methods used to find information on a person's genetic makeup. Genetic Screening
A fiberoptic device that can be inserted into the womb to take pictures of the unborn child. Fetoscope
Medical test using amniotic flued to determinethe sex and health of an unborn child, including possible genetic defects. Amniocentesis
The mechanical placement of sperm into a female's reproductive organs. Artificial Insemination
The man who supplies the sperm for the zygote of a child. Biological Father
The union of sperm and egg in an artificial setting, usually in a laboratory. In Vitro Fertilization
The woman who supplies the ovum for the zygote of a child. Biological Mother
A woman who nurtures and brings to birth from her womb a child for which she did not provide the ovum. Surrogate Mother
Created by: SPing
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