Chapter 2 - Heredity, Prenatal Dev, & Birth Flashcards
Genes
Specific sequence of nucleotides
recipes for making proteins.
Located on the chromosomes and there are an estimated 20,500 genes for humans. 
Human cells
46 chromosomes (23 pairs; one from each parent) in nucleus of the cell
Mitosis
Process by which most cells of the body are created.
The cell’s nucleus making an exact copy of all the chromosomes and splitting them into two new cells
Meiosis
Gamete’s Chromosomes duplicate, and then divide twice resulting in four cells containing only half the genetic material of the original gamete.
Each sperm and the egg process is only 23 chromosomes and combine to produce the normal 46. 
Gamete
Sperm or ova - cells used in sexual reproduction
Genotype
Sum total of all the genes a person inherits
Phenotype
Features that are actually expressed (What you see in the mirror)
Homozygous
The same version of a gene from our mother and father
Heterozygous
Different version of the gene from each parent
Dominant
Genes that express themselves in the phenotype even when paired with a different version of the chain
Recessive
Genes that express themselves only one paired with a similar version gene
Alleles
Different versions of a gene
Polygenic
Characteristics that are the result of several genes
Incomplete dominance
When the dominant gene does not completely suppress the recessive gene
Carriers
Those who have inherited only one recessive gene
Monozygotic
Identical twins
Fertilized egg splits apart in the first two weeks of development
Dizygotic
Fraternal twins
Two eggs or ova are released and fertilized by two separate sperm
Sex-linked
Defective gene is found on the X chromosome
Males have only one X chromosome so are at greater risk for sex linked disorders due to a recessive gene such as hemophilia, color blindness, and baldness
Chromosomal abnormality
Occurs when a child inherits too many or too few chromosomes.
Most common is impaired 21. Trisomy 21 or down syndrome
Down syndrome
Occurs when there are three rather than two 21st chromosomes.
Intellectual disability and possesses certain physical features, such as short fingers and toes, folds of skin over the eyes, and a protruding tongue
Sex-linked chromosomal abnormality
23rd pair
XXY, XYY, XXX, XO
Most common: Turner syndrome & Klinefelter syndrome
Turner syndrome
Occurs when part or all of one of the X chromosomes is lost and the resulting zygote has an XO composition
Affects individuals cognitive functioning and sexual maturation. External genitalia appear normal, but breast and ovaries do not develop fully and the woman does not menstruate 
Klinefelter syndrome
XXY
Results when an extra X chromosome is present in the cells of a male. 1 in 650 live male births.
The Y chromosome stimulates the growth of male genetalia, but the additional X chromosome inhibits this development. Individual typically has small testes, some breast development, and fertility, and low levels of testosterone.
Genetic counseling
Service that assist individuals identify, test for, and explain potential genetic conditions that could adversely affect themselves or their offspring
Behavioral genetics
Scientific study of the interplay between the genetic and environmental contributions to behavior
Genotype-environmental correlations
Process by which genetic factors contribute to variations in the environment
Passive
Evocative
Active 
Passive genotype-environment correlation
When children passively inherit the genes and the environments their family provides
Ex. Water skiing
Evocative genotype-environment correlation
How the social environment reacts to individuals based on their inherited characteristics
Ex. Outgoing or shy affects how you’re treated
Active genotype-environment correlation
When individuals seek out environments that support their genetic tendencies
Musically inclined seek out music instruction or what facilitates natural ability 
Genotype-environment interactions
Genetic susceptibility to environment.
Children exhibit significantly fewer behavior problems when their adoptive parents use more structure to parenting then unstructured.
Epigenetics
Studies modifications in DNA that affect gene expression and are passed on when the cells divide.
Environmental factors such as nutrition, stress, and teratogens are thought to change gene expression by switching genes on and off.
Prenatal development
Germinal period
Embryonic period
Fetal period