-
Phenotypes
observable characteristics
-
genotype
the complex blend of genetic information that determines our species and influences all our unique characteristics
-
Chromosomes
rodlike structures which store and transmit genetic information
-
DNA
chemical that chromosomes are made of
-
gene
segment of DNA along the length of the chromosome
-
Mitosis
a unique feature of DNA that it can duplicate it self
-
gametes
sex cells-- the sperm and ovum
-
meiosis
division process through which gametes are formed, which halves the number of chromosomes normally present in cell bodies
-
zygote
results from when the sperm and ovum unite at conception
-
crossing over
chromosomes next to each other break over at one or more points along their length and exchange segments so that genes from one are replaced by genes from another
-
autosomes
(meaning not sex chromosomes) n22 matching pairs of chromosomes, which geneticists number from longest (1) to shortest (22)
-
fraternal or dizygotic twins
the most common type of multiple birth, resulting from the release and fertilization of two ova
-
monozygotic twins
a zygote that has started to duplicate separates into two clusters of cells that develop into two individuals
-
allele
gene that forms when two forms of a gene occur at the same place on the chromosomes one inherited from the mother and one from the father
-
homozygous
if the alleles from both parents are alike, and the child will display the inherited trait
-
heterozygous
when alleles are different, and the relationship between alleles determine the phenotype
-
dominant recessive inheritance
occurs when only one allele affects the child's characteristics
-
carriers
when a heterozygous individual passes the recessive allele on to their children
-
modifier genes
enhance or dilute the effects of other genes
-
incomplete dominance
a pattern of inheritance in which both alleles are expressed in the phenotype, resulting in a combined trait, or one that is intermediate between the two
-
X-linked inheritance
when a harmful allele is carried on the X chromosome, males are more likely to be affected because their sex chromosomes don't match
-
genomic imprinting
alleles are imprinted, or chemically marked, in such a way that one pair member is activated regardless of its makeup
-
mutation
a sudden but permanent change in a segment of DNA
-
polygenic inheritance
in which many genes affect the characteristic in question
-
Down syndrome
the most common chromosomal disorder
-
Genetic counseling
a communication process designed to help couples asses their chances of giving birth to a baby with a hereditary disorder and choose the best course of action in view of risk and family goals
-
prenatal diagnostic methods
medical procedures that permit detection of developmental problems before birth
-
coparenting
mutually supporting each others parenting behaviors
-
Socio economic status
- combines 3 vairables 1. years of education
- 2. prestige of ones job an skill it requires
- income
-
subcultures
groups of people with beliefs and customs that differ from those of the larger culture
-
extended family households
parent and child live with one or more adult relative
-
collectivist societies
people define themselves as part of a croup and stress group over individual goals
-
individualistic societies
people think of themselves as separate entities and are largely concerned with their own personal needs
-
Public policies
laws and gov programs designed to improve current conditions
-
behavioral genetics
is a field devoted to uncovering the contributions of nature and nurture to this diversity in human traits and abilities
-
heritability estimates
measure the extent to which individual differences in complex traits in a specific population are due to genetic factors
-
kinship studies
compare characteristics of family members
-
range of reaction
each person's unique genetically determined response to the environment
-
canalization
the tendency of heredity to restrict the development of some characteristics to just one or a few outcomes
-
genetic-environmental correlation
our genes influence the environments to which we are exposed
-
niche-picking
the tendency to actively choose environments that complement our heredity
-
epigenesis
development resulting from ongoing bidirectional exchanges between heredity an all levels of the environment
|
|