Chapter 3: Conception, Heredity, and Environment
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Complete list of Terms and Definitions for Chapter 3: Conception, Heredity, and Environment

Terms Definitions
Dominant Inheritance Pattern of inheritance in which, when a child receives different alleles, only the dominant one is expressed.
Heterozygous Possessing differing alleles for a trait.
Down Syndrome Chromosomal disorder characterized by moderate-to-severe mental retardation and by such physical signs as downward-sloping skin fold at inner corners of the eyes.
Reaction Range Potential variability depending on environmental conditions, in the expression of a heredity trait.
Deoxyribonucleic Acid (DNA) Chemical that carried inherited instructions for the development of all cellular forms of life.
Assisted Reproductive Technology (ART) Methods used to achieve conception through artificial means.
Genotype-Environment Correlation Tendency of certain genetic and environmental influences to reinforce each other; may be passive, reactive (evocative), or active.
Nonshared Environmental Effects The unique environment in which each child grows up, consisting of distinctive influences or influences that affect one child differently than another.
Schizophrenia Neurological disorder marked by loss of contact with reality; hallucinations and delusions; loss of coherent, logical thought; and inappropriate emotionality.
Autosomes In humans, the 22 pairs of chromosomes not related to sexual expression.
Genes Small segments of DNA located in definite positions on particular chromosomes; functional units of heredity.
Behavioral Genetics Quantitative study of relative heredity and environmental influences on behavior.
Fertilization Union of sperm and ovum to produce a zygote; also called conception.
Genotype Genetic makeup of a person, containing both expressed and unexpressed characteristics.
Homozygous Possessing two identical alleles for a trait.
Genetic Counseling Clinical service that advises prospective parents of their probably risk of having children with genetic defects.
Alleles Two or more alternative forms of a gene that can occupy the same position on paired chromosomes and affect the same trait.
Polygenic Inheritance Pattern of inheritance in which multiple genes at different sites on chromosomes affect a complex trait.
Zygote One-cell organism resulting from fertilization.
Sex-Linked Inheritance Pattern of inheritance in which certain characteristics carried on the X chromosomes inherited from the mother are transmitted differently to her male and female offspring.
Temperament Characteristic disposition, or style of approaching and reacting to situations.
Concordant Term describing the tendency of twins to share the same trait or disorder.
Canalization Limitation on variance of expression of certain inherited characteristics.
Mutations Permanent alterations in genes or chromosomes that usually produce harmful characteristics.
Obesity Extreme overweight in relation to age, sex, heigh, and body type.
Phenotype Observable characteristics of a person.
Multifactorial Transmission Combination of genetic and environmental factors to produce certain complex traits.
Sex Chromosomes Pair of chromosomes that determines sex, XX in a normal female, XY in a normal male.
Genetic Code Sequence of bases within the DNA molecule; a set of rules that govern the formation of proteins that determine the structure and functions of living cells.
Infertility Inability to conceive after 12 months of trying.
Recessive Inheritance Pattern of inheritance in which a child receives identical recessive alleles, resulting in expression of a nondominant trait.
Epigenises Mechanism that turns genes on or off and determines functions of body cells.
Heritability Statistical estimate of contribution of heredity to individual differences in a specific trait within a given population at a particular time.
Incomplete Dominance Pattern of inheritance in which a child receives two different alleles, resulting in partial expression of a trait.
Chromosomes Coils of DNA that consists of genes.
Human Genome The complete sequence of genes in the human body.