Glossary Chapter 2 Flashcards
(35 cards)
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 that
are organized in 23 pairs.
chromosomes
twins who are genetically identical.
monozygotic twins
twins who are produced when two separate ova are fertilized by two separate sperm at roughly the same time.
dizygotic twins
the one trait that is expressed
when two 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
an 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
genes that are considered
recessive and located only 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 twenty-first pair; once referred to as mongolism.
Down syndrome
a disorder produced by injury to a gene 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 (bulan sabit).
sickle-cell anemia
a disorder that produces blindness
and muscle degeneration prior to
death; there is no treatment (nyerang nervous system)
Tay-Sachs disease
a disorder resulting from the presence of an extra X chromosome that produces underdeveloped genitals, extreme height, and
enlarged breasts.
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 mother’s
womb to produce an image of
the unborn baby, whose 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
patterns of arousal and
emotionality that represent
consistent and enduring
characteristics in an individual.
temperament