Table of Contents | Bibliography
A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z
albino: Having pale or colorless skin, eyes, and hair because the body does not produce enough pigment.
alpha-fetoprotein test (AFP): A prenatal test to measure the amount of a fetal protein in the mother's blood. Abnormal amounts of the protein may indicate genetic problems in the fetus.
Americans with Disabilities Act (ADA): A 1990 federal law that forbids discrimination against persons who are disabled.
amniocentesis: A prenatal test in which cells surrounding a fetus are removed in order to examine the chromosomes.
artificial insemination: The injection of semen into a woman's uterus (not through sexual intercourse) in order to make her pregnant.
bacteria: Very small, single-celled life-forms that can reproduce quickly.
bases: Distinct chemical ingredients found in the genetic material of all life-forms.
behavioral genetics: The study of whether and how traits for behavior are inherited.
biotechnology: The use of living things to make products.
carcinogens: Cancer-causing substances.
carrier: A person who has one copy of the gene mutation for a recessive disorder. Carriers are not affected by the disorder. However, they can pass on the mutated gene to their children. Children who inherit two such genes may be affected by the disorder.
chorionic villus sampling (CVS): A prenatal test in which cells surrounding an embryo are removed in order to examine the chromosomes.
chromosomes: Separate strands of genes, contained in the nucleus of a cell. Normally, chromosomes appear in corresponding pairs. A genome is made up of a complete set of paired chromosomes.
clone: To make an exact copy of.
conception: In reproduction, the point at which a sperm fertilizes an egg.
crossing over: Where a section of one chromosome switches places with the same section from the other chromosome of the pair. This sometimes occurs when a germ cell makes copies of its chromosomes before dividing.
cystic fibrosis (CF): A recessive genetic disorder affecting the mucus lining of the lungs, leading to breathing problems and other difficulties.
data bank: A collection of information organized so that specific facts can be retrieved as needed. Today, many data banks are organized on computers.
disorders: Problems in how the body functions. Health problems caused by mutations in the genes are referred to as genetic disorders.
DNA: The material inside the nucleus of cells that carries genetic information. The scientific name for DNA is deoxyribonucleic acid.
DNA fingerprinting: A term for DNA typing. (See below.)
DNA marker: A gene or other fragment of DNA whose location in the genome is known.
DNA typing: The analysis of sections of DNA for purposes of identification.
dominant: Having power and influence. In genetics, a dominant gene is a gene that expresses its instructions.
embryo: An animal in the early stage of development before birth. In humans, the embryo stage is the first three months following conception.
environment: The nongenetic conditions and circumstances that affect a person's conduct and health.
enzymes: Proteins that trigger activity in the cells of the body. An enzyme is not affected by the activity that it sets off.
ethical issues: Questions concerning what is moral or right.
eugenics: The belief that information about heredity can be used to improve the human race.
evolution: The process by which all forms of plant and animal life change slowly over time because of slight variations in the genes that one generation passes down to the next.
ex utero genetic testing: DNA analysis performed on cells of eggs that have been fertilized in vitro.
fetus: An animal in the later stage of development before birth. In humans, the fetal stage is the from the end of the third month until birth.
genes: Units of hereditary information. Genes contain the instructions for the production of proteins, which make up the structure of cells and direct their activities.
gene therapy: The altering of genes in order to affect their function.
genetic counseling: Education and guidance offered by professional advisors in order to help people make informed decisions based on genetic knowledge. Genetic counseling is intended to help a person understand the meaning of specific information about his or her genes. It also is intended to help a person decide whether to have a genetic test performed or what to do with information provided by such a test.
genetic determinism: The false belief that a person's fate is determined solely by his or her genes.
genetic engineering: The artificial introduction of changes to the genes in a cell.
genetic expression: The effects of a gene's instruction on the cells of the body.
genetic linkage study: Examination of the DNA of family members to determine who may be at risk for a genetic disorder occurring in the family tree. Doctors look for variations that consistently appear in the DNA of family members with the disorder. These DNA variations may or may not be related to the genetic disorder. However, if they appear in the DNA of another family member, it can indicate the person's risk of inheriting the disorder.
genetic profile: A collection of information about a person's genes.
genetics: The field of science that looks at how traits are passed down from one generation to another, through the genes.
genome: The complete package of genetic material for a living thing, organized in chromosomes. A copy of the genome is found in most cells.
germ cells: The cells of the body involved in reproduction. Sperm of the male and eggs of the female are formed from germ cells.
germ-line therapy: The altering of genes in reproductive cells (sperm or egg) in order to affect their function in any offspring that may be created.
heredity: The handing down of certain traits from parents to their offspring. The process of heredity occurs through the genes.
hormones: Proteins produced by organs of the body that trigger activity in other locations.
Human Genome Project: The scientific mission to "read" the order of bases as they appear in the DNA of human chromosomes. The Human Genome Project actually is not one project, but rather many hundreds of separate research projects being conducted throughout the world. The objective is to create a directory of the genes that can be used to answer questions such as what specific genes do and how they work.
Huntington's disease (HD): A dominant genetic disorder in which a protein is produced abnormally, leading to the breakdown in the parts of the brain that control movement.
immune disorders: Health problems caused by the fact that the body cannot properly fight infection.
in vitro fertilization: The mixing of eggs with sperm in a laboratory dish in order to achieve conception.
karyotype: A picture of the chromosomes in a cell that is used to check for abnormalities. A karyotype is created by staining the chromosomes with dye and photographing them through a microscope. The photograph is then cut up and rearranged so that the chromosomes are lined up into corresponding pairs.
legal issues: Questions concerning the protections that laws or regulations should provide.
mutation: Changes that occur to the order of bases appearing in the DNA inside a cell.
nucleus: The central part of a cell where the chromosomes are contained.
parasites: Plants or animals that live off another creature (or even inside it), obtaining food and protection without offering any benefit in return.
paternity: Identification of the father of a child.
pigment: The dyelike material in cells that provides color to skin, eye and hair.
prenatal: Before birth.
privacy: The condition of being left alone, out of public view and in control of information that is known about you.
proteins: The basic chemicals that make up the structure of cells and direct their activities.
recessive: Moving back and out of view. In genetics, a recessive gene is a gene that does not express its instructions when paired with a dominant gene.
reproductive technology: The application of scientific knowledge to assist in making babies.
selective breeding: The selection of certain seeds or animals for reproduction in order to influence the traits inherited by the next generation.
severe combined immunodeficiency (SCID): An immune disorder in which the body does not produce the special blood cells that resist infection.
sickle cell anemia: A recessive genetic disorder in which red blood cells take on an unusual shape, leading to other problems with the blood.
social issues: Questions concerning how events may affect society as a whole and individuals in society.
species: A single, distinct class of living creature with features that distinguish it from others.
temperament: A person's way of responding to the world. Examples of temperament include shy, bold, risk taking, and cautious.
traits: Ways of looking, thinking, or being. Traits that are genetic are passed down through the genes from parents to offspring.
transgenic: Containing genes from another species.
ultrasound imaging: A technique for looking inside the body by using sound waves to create images.
viruses: Extremely small and simple life-forms, made merely of a protein shell and a genome. A virus reproduces by inserting its genome into the cells of other life-forms. As those cells duplicate, so does the virus.
Your Genes, Your Choices is a publication of Science + Literacy for Health, a project of the AAAS Directorate for Education and Human Resources. The publication was funded by the U.S. Department of Energy. The website was built by Mike Wooldridge. Send feedback to SciLit@aaas.org.