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29 Cards in this Set

  • Front
  • Back
The molecular basis of heredity, constructed of a double helix whose parallel strands consist of both pairs held together by hydrogen bonds
DNA (deoxyribonucleic acid)
A carrier of genes; one of the 46 molecules of DNA (in 23 pairs) that each cell of the body contains and that, together, contain all human genes
chromosome
The full set of chromosomes, with all the genes they contain, that make up the genetic material of an organism
genome
The basic unit for the trasmission of heredity instructions
gene
A reproductive cell; that is, a cell that can reproduce a new individual if it combines with one from the other sex
gamete
The single cell formed from the fusing of a sperm and an ovum
zygote
An organism's entire genetic inheritance, or genetic potential
genotype
A slight, normal variation of a particular gene
allele
The chromosome pair that, in humans, determines the zygote's sex, amoung other things
23rd pair
A 23rd pair that consists of two X-shaped chromosomes, one from the mother and one from the father
XX
A 23rd pair that consists of one X-shaped chromosome from the mother and one Y-shaped chromosome from the father
XY
The naturally occurring termination of a pergnancy before the fetus is fully developed
spontaneous abortion or miscarriage
Twins who have identical genes because they were formed from one zygote that split into two identical organisms very early in development
monozygotic twins
Twins who were formed when two seperate ova were fertilized by two separate sperm at roughly the same time. Such twins share about half their genes, like any other sibilings
dizygotic twins
Processes in which certain genes code for proteins that switch other genes on and off, making sure that the other genes produce proteins at the appropriate times
on-off switching mechanism
A person's actual apperance and behavior, which are the result of both genetic and environmental influences.
phenotype
Referring to inherited traits that are influenced by many factors, including factors in the environment, rather than by genetic influences alone
multifactorial
Referring to inherited traits that are influenced by many genes, rather than by a single gene
polygenic
A gene that, through interaction with other genes, affects a specific trait
additive gene
The interaction of a pair of alleles in such a way that the phenotype reveals the influence of one allele (the dominant gene) more than that of the other (the recessive gene).
dominant-recessive pattern
The member of an interacting pair of alleles whose influence is more evident in the phenotype
dominant gene
The member of an interacting pair of alleles whose influence is less evident in the phenotype
recessive gene
Referring to a gene that is located on the X chromosome
X-Linked
An international effort to map the complete human genetic code
Human Genome Project
A person whose genotype includes a gene that is not expressed in his or her phenotype but can be passed on to his or her children
carrier
The study of the genetic origins of psychological characteristics, such as personality patterns, psychological disorders, and intellectual abilities
behavior genetics
Referring to a condition in which a persona has a mixture of cells, some normal and some with the incorrect number of chromosomes
mosaic
A genetic disorder in which part of the X chromosome is attached to the rest of it by a very thin string of molecules' often produces mental deficiency in males who inherit it
fragile X syndrome
A process of consultation and testing that enables individuals to learn about their genetic heritage, including conditions that might harm any children they may have
genetic counseling