Chapter 3 Flashcards

1
Q

Union of sperm and ovum to produce a
zygote; also called conception.

A

fertilization

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2
Q

One-celled organism resulting from
fertilization.

A

zygote

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3
Q

Twins conceived by the union of two
different ova (or a single ovum that has
split) with two different sperm cells; also
called fraternal twins; they are no more
alike genetically than any other siblings.

A

dizygotic twins

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4
Q

Twins resulting from the division of a
single zygote after fertilization; also
called identical twins; they are
genetically similar.

A

monozygotic twins

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5
Q

Chemical that carries inherited
instructions for the development of all
cellular forms of life.

A

deoxyribonucleic acid (DNA)

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6
Q

Sequence of bases within the DNA
molecule; governs the formation of
proteins that determine the structure
and functions of living cells.

A

genetic code

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7
Q

Coils of DNA that consist of genes.

A

chromosomes

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8
Q

Small segments of DNA located in definite
positions on particular chromosomes;
functional units of heredity

A

genes

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9
Q

Complete sequence of genes in the
human body.

A

human genome

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10
Q

Permanent alterations in genes or
chromosomes that may produce
harmful characteristics.

A

mutations

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11
Q

In humans, the 22 pairs of chromosomes
not related to sexual expression.

A

autosomes

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12
Q

Pair of chromosomes that determines
sex: XX in the normal human female,
XY in the normal human male.

A

sex chromosomes

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13
Q

Two or more alternative forms of a gene
that occupy the same position on
paired chromosomes and affect the
same trait.

A

alleles

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14
Q

Possessing two identical alleles for a trait.

A

homozygous

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15
Q

Possessing differing alleles for a trait.

A

heterozygous

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16
Q

Pattern of inheritance in which, when a
child receives different alleles, only the
dominant one is expressed.

A

dominant inheritance

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17
Q

Pattern of inheritance in which a child
receives identical recessive alleles,
resulting in expression of a nondominant
trait.

A

recessive inheritance

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18
Q

Pattern of inheritance in which multiple
genes at different sites on
chromosomes affect a complex trait.

A

polygenic inheritance

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19
Q

Observable characteristics of a person.

A

phenotype

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20
Q

Genetic makeup of a person, containing
both expressed and unexpressed
characteristics.

A

genotype

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21
Q

Combination of genetic and
environmental factors to produce
certain complex traits.

A

multifactorial transmission

22
Q

Mechanism that turns genes on or off
and determines functions of body cells.

A

Epigenesis

23
Q

Pattern of inheritance in which a child
receives two different alleles, resulting
in partial expression of a trait.

A

incomplete dominance

24
Q

Pattern of inheritance in which certain
characteristics carried on the X
chromosome inherited from the mother
are transmitted differently to her male
and female offspring.

A

sex-linked inheritance

25
Chromosomal disorder characterized by moderate-to-severe mental retardation and by such physical signs as a downwardsloping skin fold at the inner corners of the eyes. Also called trisomy-21.
Down syndrome
26
Clinical service that advises prospective parents of their probable risk of having children with hereditary defects.
Genetic counseling
27
Quantitative study of relative hereditary and environmental influences on behavior.
behavioral genetics
28
Statistical estimate of contribution of heredity to individual differences in a specific trait within a given population.
heritability
29
Term describing tendency of twins to share the same trait or disorder.
concordant
30
Potential variability, depending on environmental conditions, in the expression of a hereditary trait.
reaction range
31
Limitation on variance of expression of certain inherited characteristics.
canalization
32
The portion of phenotypic variation that results from the reactions of genetically different individuals to similar environmental conditions.
genotype-environment interaction
33
Tendency of certain genetic and environmental influences to reinforce each other; may be passive, reactive (evocative), or active. Also called genotype-environment covariance.
genotype-environment correlation
34
Tendency of a person, especially after early childhood, to seek out environments compatible with his or her genotype.
niche-picking
35
The unique environment in which each child grows up, consisting of distinctive influences or influences that affect one child differently than another.
nonshared environmental effects
36
Extreme overweight in relation to age, sex, height, and body type as defined by having a body mass index at or above the 95th percentile.
Obesity
37
Characteristic disposition, or style of approaching and reacting to situations.
Temperament
38
Mental disorder marked by loss of contact with reality; symptoms include hallucinations and delusions.
schizophrenia
39
Period of development between conception and birth.
Gestation
40
Age of an unborn baby, usually dated from the first day of an expectant mother’s last menstrual cycle.
Gestational age
41
The upper parts of the body develop before the lower parts of the trunk.
cephalocaudal principle
42
The parts of the body near the center develop before the extremities.
proximodistal principle
43
First 2 weeks of prenatal development, characterized by rapid cell division, blastocyst formation, and implantation in the wall of the uterus.
Germinal stage
44
The attachment of the blastocyst to the uterine wall, occurring at about day 6.
Implantation
45
Second stage of gestation (2 to 8 weeks), characterized by rapid growth and development of major body systems and organs.
embryonic stage
46
Natural expulsion from the uterus of an embryo that cannot survive outside the womb; also called miscarriage.
spontaneous abortion
47
Final stage of gestation (from 8 weeks to birth), characterized by increased differentiation of body parts and greatly enlarged body size.
Fetal stage
48
Prenatal medical procedure using highfrequency sound waves to detect the outline of a fetus and its movements, so as to determine whether a pregnancy is progressing normally
Ultrasound
49
Environmental agent, such as a virus, a drug, or radiation, that can interfere with normal prenatal development and cause developmental abnormalities.
Teratogen
50
Combination of mental, motor, and developmental abnormalities affecting the offspring of some women who drink heavily during pregnancy
fetal alcohol syndrome (FAS)
51
Viral disease that undermines effective functioning of the immune system.
acquired immune deficiency syndrome (AIDS
52
Physical or psychological demands on a person or organism.
Stress