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Feldman DevPsy ch 2

The Start of Life: Prenatal Development

TermDescription
genes basic unit of genetic information
DNA substance that genes are composed of that determine the nature of every cell in the body and how it will function
chromosomes rod shaped portion of DNA that are organized in 23 pairs
zygote the new cell fromed by the process of fertilization
gametes the sex cells from the mother and father that form a new cell at conception
ononzygotic twins twins who are genetically identical
dizygotic twins twins who are produced when two separate ova are fertilized by two separate sperm at roughly the same time
dominate trait the one trait that is expressed when two competing traits are present
recessive trait a trait within an organism that is present but not expressed
genotype the underlying combination af genetic material present but not outwardly visible in an organism
phenotype an observable trait
homozygous inheriting from parents similar genes for a given trait
heterozygous inheriting from parents different forms of a gene for a given trait
polygenic inheritance inheritance in which a combination of multiple gene paris is responsible for the production of a particular trait
x linked genes genes that are considered recessive and located only on the x chromosome
behavioral genetics the study of the effects of heredity on behavoir
down syndrome a disorder produced by the presence of an extra chromosome on the 21st pair (monoglism)
fragile X syndrome a disorder produced by injury to a gene on the x chromosome producing mild to moderate mental retardation
sickel-cell anemia blood disorder taht gets its name for the shape of the red blood cells in those who have it
Tay-Sachs disease disorder that produces blindness and muscle degeneration prior to death, no treatment
Klienfetler's syndrome disorder resultion from the presence of an extra chromosome that produces underdeveloped genitals, extreme height, and enlarged breasts
genetic counseling discipline that focuses on helping people deal with issues relating to inherited disorders
amniocentisis the process of identifying genetic defects by examining a small sample of fetal cells drawn by a needle inserted into the amniotic fluid surrounding the unborn fetus
chorinic vilus sampling (CVS) test used to find genetic defects that involves taking samples of hairlike material that surrounds the embryo
ultrasound sonography process in which high frequency sound waves scan the mother's womb to produce and image of the unborn baby, whose size and shape can then be assessed
Created by: eestrand
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