Chapter 2 Flashcards
The new cell formed by the process of fertilization.
Zygote
The basic units of genetic information
Genes
The substance that genes are composed of that determines the nature of every cell in the body and how it will function.
DNA (deoxyribonucleic acid) molecules
Rod shaped portions of DNA better organized in 23 pairs
Chromosomes
Twins who are genetically identical
Monozygotic twins
Twins were produced went to separate ova are fertilized by two separate sperm at roughly the same time.
Dizygotic twins
The one trait that is expressed went to competing traits are present
Dominant trait
A trait within an organism that is present, but is not expressed.
Recessive trait
The underlying combination of genetic material present (but not outwardly visible) in an organism
Genotype
And observable trait; the trait that is actually seen
Phenotype
Inheriting from parents similar genes for a given trait.
Homozygous
Inheriting from parents different forms of a gene for a given trait.
Heterozygous
Inheritance in which a combination of multiple gene pairs is responsible for the production of a particular trait.
Polygenetic inheritance
Jeans that are considered recessive it located on the X chromosome.
X-linked genes
The study of the effects of heredity on behavior and psychological characteristics
Behavioral genetics
A disorder produced by the presence of an extra chromosome on the 21st pair; once referred to as mongolism.
Down syndrome
A disorder produced by injury to Regina on the X chromosome, producing mild to moderate mental retardation
Fragile X syndrome
A blood disorder that gets its name from the shape of the red blood cells in those who have it.
Sickle cell anemia
I just ordered that produces blindness and muscle degeneration prior to death; there’s no treatment.
Tay-Sachs disease
A disorder resulting from the presence of an extra X chromosome that produces underdeveloped genitals, extreme high, and enlarged breast.
Klinefelter’s syndrome
The discipline that focuses on helping people deal with issues relating to inherited disorders.
Genetic counseling
A process in which high-frequency sound waves scan the mothers womb to produce an image of the unborn baby, who size and shape can then be assessed.
Ultrasound sonography
A test used to find genetic defects that involves taking samples of hair like material that surrounds the embryo.
Chorionic villus sampling (CVS)
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.
Amniocentesis