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33 Cards in this Set

  • Front
  • Back

Behavioral genetics

Research to determine the degree of genetic basis for a behavior, a trait, or an ability

Molecular genetics

Research focused on the identification of particular genes to identify how these genes work within the cell

Chromosomes

The strands of genes that constitute the human genetic endowment

Fertilization

The union of a father's sperm and the mother's egg to produce a zygote

Zygote

A fertilized egg

Genome

The complete sequence of bases that make up the genetic instructions of an organism

Mutations

Change in the formation of genes that occur as cells divide

Nucleotide

An organic molecule that contains one of the four bases with a phosphate group and a sugar molecule

Dominant genes

Genes that are usually expressed in the phenotype

Recessive genes

Genes that are generally not expressed in the phenotype unless paired with another

Genotype

The genes that are present at a particular location on the chromosome

Phenotype

The genetically based characteristics that are actually shown in one's body

Polygenic inheritance

Numerous genes that may interact together to promote any particular trait or behavior

Pleiotropic effects

The many different influences any single Gene may have

Generalist genes

Genes that affect many, apparently distinct cognitive abilities

Single Gene disorders

Genetic disorders caused by a single recessive gene or mutation

Chromosome disorders

Disorders that result when too many or too few chromosomes are formed or when there is a change in the structure of the chromosome caused by breakage

Multifactorial inheritance disorders

Disorders that result from many genes in interaction with environmental influences

Amniocentesis

A testable for genetic abnormalities prenatally, in which a physician uses a long, thin needle to extract amniotic fluid, which is then tested

Chorionic villus sampling (CVS)

A test to look for genetic abnormalities prenatally, in which a small tube is inserted either through the vagina and cervix or through a needle inserted in the abdomen, and the sample of cells is retrieved from the chorion for testing

Chorion

The outer fetal membrane that surrounds the fetus and gives rise to the placenta

Gene therapy

Treatment of genetic disorders through implanting or disabling specific genes

Heritability

A measure of the extent to which genes determine a particular Behavior or characteristic

Concordance rate

The degree to which a trait or an ability of one individual is similar to that of another:


Used to examine similarities between twins and among adopted children and their biological and adoptive parents

Dizygotic (DZ) twins

Twins formed when a woman produces two ova or eggs, which are fertilized by two sperm genetically.



Are as similar as any siblings

Monozygotic (MZ) twins

Formed when a woman produces one egg that is fertilized by one sperm and the resulting ball of cells then splits to form two individuals with the same genes

Canalization

The degree to which the expression of a gene is influenced by the environment



How the same phenotypes are produced by a genotype even though the environment may differ

Epigenetics

A system by which genes are activated or silenced in response events or circumstances in the individuals environment

Passive gene-environment

A situation in which a child's family shares his own genetically determined abilities and interests

Active gene-environment interaction

When one's genetic endowment becomes a driving force for children to seek out experiences that fit their genetic endowment

Evocative gene-environment

When children's genetic endowment cause them to act in a way that draws out or "evokes" certain responses from those around them

Down syndrome

One extra 21st chromosome



Symptoms include intellectual disability, typical facial features, poor muscle tone, possible problems with heart, digestion, and hearing



Physical, occupational, speech, and educational therapy. Medical intervention as needed

Trisomy

A genetic disorder in which a person has three copies of a chromosome instead of two.