WK1 Chapter 2 Genetics & Prenatal Dev Flashcards

1
Q

sausage-shaped structure in the nucleus of
cels, containing genes, which are paired,
except in reproductive cels

A

chromosome

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2
Q

the human body contain —– chromosomes in —–
pairs, with one chromosome in each pair inherited from the mother
and the other inherited from the father

A

46, 23 pairs

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3
Q

DNA

A

(deoxyribonucleic acid)
long strand of cel material that stores and
transfers genetic information in a l life forms

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4
Q

segment of DNA containing coded
instructions for the growth and functioning of
the organism

A

gene

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5
Q

entire store of an organism’s hereditary
information

A

genome

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6
Q

What would the genome of a female and a males 23rd pair of chromosones be

A

Male: XY

Female: XX

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7
Q

be XY rather than XXif you were born with a
genotype that included exceptional musical ability, this talent might
never be developed if

A

your environment provided no access to
musical instruments or musical instruction.

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8
Q

organism’s unique genetic inheritance

A

genotype

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9
Q

organism’s actual characteristics, derived
from its genotype

A

phenotype

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10
Q

on a pair of chromosomes, each of two forms
of a gene

A

allele

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11
Q

alleleRecessive genes are expressed in the phenotype only
when

A

they are paired with another recessive gene

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12
Q

——– - ——— ———- occurs when only one of the two genes—the dominant gene—influences the
phenotype, whereas the recessive gene does not, even though it is part of the genotype

A

dominant–recessive inheritance

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13
Q

pattern of inheritance in which a pair of
chromosomes contains one dominant and one
recessive gene, but only the dominant gene is
expressed in the phenotype

A

dominant–recessive inheritance

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14
Q

form of dominant–recessive inheritance in
which the phenotype is influenced primarily by
the dominant gene but also to some extent by
the recessive gene

A

incomplete dominance

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15
Q

polygenic inheritance
expression of phenotypic characteristics due
to the interaction of multiple genes

A

polygenic inheritance

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16
Q

chromosomes that determine whether an
organism is male (XY) or female (XX)

A

sex chromosomes

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17
Q

eggs in the mother contain an —– chromosome but
sperm may carry —– chromosome

A

X

either an X or a Y

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18
Q

males more vulnerable than females to a variety of recessive
disorders that are linked to the — ————-

A

X chromosome

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19
Q

Why can a woman be a carrier of a disorder to the next generation but will not have the disorder herself.

A

It may be disorders that are linked to the X chromosome. If a female has one X
chromosome that contains the recessive gene for a disorder, the disorder will not show up in her phenotype because the dominant
gene on her other X chromosome will prevent it from being expressed.

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20
Q

Whay are men more vulnerable to X chromosome linked disorders?

A

because he has no other X chromosome that may contain a dominant gene to block its expression and the Y chromosone can not provide this function

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21
Q

pattern of inheritance in which a recessive
characteristic is expressed because it is
carried on the male’s X chromosome

A

X-linked inheritance

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22
Q

Because of X-linked inheritance, males are at greater risk of

A

a
wide variety of genetically based conditions, including learning disabilities and intellectual disability

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23
Q

field in the study of human development that
aims to identify the extent to which genes
influence behaviour, primarily by comparing
people who share different amounts of their
genes

A

behaviour genetics

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24
Q

twins who developed from a single ova and
sperm, and therefore have exactly the same
genotype; also called identical twins

A

monozygotic (MZ) twins

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25
twins that result when two ova are released by a female instead of one, and both are fertilised by different sperm; also called fraternal twins
dizygotic (DZ) twins
26
statistical estimate of the extent to which genes are responsible for the differences among people within a specific population, with values ranging from 0 to 1.00
heritability
27
degree of similarity in phenotype among pairs of family members, expressed as a percentage
concordance rate
28
heritability estimates measure --------- rather than --------.
phenotype rather than genotype.
29
in development, the continuous bidirectional interactions between genes and environment
epigenesis
30
range of possible developmental paths established by genes; environment determines where development takes place within that range
reaction range
31
in the theory of genotype S environment effects, the type that results from the facthat in a biological family, parents provide both genes and environment to their children
passive genotype → environment effects
32
the type that results when a person’s inherited characteristics evoke responses from others in the environment in the theory of genotype → environment effects,
evocative genotype → environment effects
33
the type that results when people seek out environments that correspond to their genotypic characteristics in the theory of genotype → environment effects,
active genotype → environment effects
34
cells, distinctive to each sex, that are involved in reproduction (egg cells in the ovaries of the female and sperm in the testes of the male)
gametes
35
mature egg that develops in ovaries, about every 28 days in human females
ovum
36
process by which gametes are generated, through separation and duplication of chromosome pairs, ending in four new gametes from the original cell, each with half the number of chromosomes of the original cell
meiosis
37
process of cel replication in which the chromosomes duplicate themselves and the cel divides into two cels, each with the same number of chromosomes as the original cel
mitosis
38
in an ovum, fluid that provides nutrients for the first 2 weeks of growth if the ovum is fertilised, until the fertilised ovum reaches the uterus and begins drawing nutrients from the mother
cytoplasm
39
at the outset of meiosis, the exchange of genetic material between paired chromosomes
crossing over
40
Because crossing over begins when ova are created, this means that the development of a unique genotype for each individual begins
before the individual’s mother is born
41
during the female reproductive cycle, the ovum plus other cels that surround the ovum and provide nutrients
follicle
42
It is only during ------- after the ovum enters the fa lopian tube that fertilisation can occur
the first 24 hours
43
fo lowing fertilisation, the new ce l formed from the union of sperm and ovum
zygote
43
Ova and sperm are caled -------, and each has -- single chromosomes.
gametes 23
44
if two ova are released by the woman instead of one, and both are fertilised by sperm, resulting in
DZ twins (dizygotic— two zygotes)
45
when a zygote that has just begun the process of cel division splits into two separate clusters of ce ls, creating:
MZ twins ( monozygotic—one zygote)
46
------- twins are less common than ------- twins
MZ twins are less common than DZ twins ( occurring about 1 in every 285 births) DZ are roughly 1 in 60
47
------ twins do not run in families
MZ (Splitting) unlike DZ twins (Two Ovum)
48
germinal period
first 2 weeks after conception
49
ball of about 100 cells formed by about 1 week following conception
blastocyst
50
in the blastocyst, the outer layer of cels, which wil go on to form structures that provide protection and nourishment to the embryo
trophoblast
51
in the blastocyst, the inner layer of cels, which wil go on to form the embryo
embryonic disk
52
fluid-fi led membrane that surrounds and protects the developing organism in the womb
amnion
53
in the womb, gatekeeper between mother and fetus, protecting the fetus from bacteria and wastes in the mother’s blood, and producing hormones that maintain the blood in the uterine lining and cause the mother’s breasts to produce milk
placenta
54
Prenatal Development Week 1-2
Gestational Period
55
Prenatal Development Week 3-8
Embryonic Period
56
structure connecting the placenta to the mother’s uterus
umbilical cord
57
in prenatal development, elapsed time since conception
gestation
58
in the embryonic period, the outer layer of cels, which wil eventualy become the skin, hair, nails, sensory organs and nervous system (brain and spinal cord)
ectoderm
59
in the embryonic period, the middle of the three cel layers, which wil become the muscles, bones, reproductive system and circulatory system
mesoderm
60
in the embryonic period, the inner layer of cels, which wil become the digestive system and the respiratory system
endoderm
61
in the embryonic period, the part of the ectoderm that wil become the spinal cord and brain
neural tube
62
cel of the nervous system
neuron
63
in prenatal development, the period from week 9 until birth
fetal period
64
at birth, babies are covered with this oily, cheesy substance, which protects their skin from chapping in the wom
vernix
65
The ---- are the last major organ to become viable
lungs
66
behaviour, environment or bodily condition that can have damaging influence on prenatal development
teratogen
67
malnutrition, infectious diseases, alcohol and tobacco
are major teratogens
68
The most common teratagon worldwide is
Malnutrition
69
folic acid, iodinne and iron are common
contributors to malnutritian in fetal development
70
behaviour, environment or bodily condition that can have damaging influence on prenatal development
teratogen
71
set of problems that occur as a consequence of high maternal alcohol use during pregnancy, including facial deformities, heart problems, misshapen limbs and a variety of cognitive problems
fetal alcohol spectrum disorder (FASD)
72
sexualy transmitted infection caused by HIV, resulting in damage to the immune system
AIDS (acquired immune deficiency syndrome)
73
genetic disorder due to carrying an extra chromosome on the 21st pair
Down syndrome
74
involving a combination of genetic and environmental factors
multifactorial
75
a permanent alteration of a DNA sequence that makes up a gene
genetic mutation
76
prenatal procedure in which a needle is used to withdraw amniotic fluid containing fetal cells from the placenta, allowing possible prenatal problems to be detected
amniocentesis
77
prenatal technique for diagnosing genetic problems, involving taking a sample of cells at 5–10 weeks gestation by inserting a tube into the uterus
chorionic villus sampling (CVS)
78
prenatal test that involves the pregnant mother giving a blood sample to test for increased risk for chromosomal abnormalities in the fetus, including Down syndrome
non-invasive prenatal testing
79
inability to attain pregnancy after at least a year of regular sexual intercourse
infertility
80
procedure of injecting sperm directly into the uterus
intrauterine insemination (IUI)
81
infertility treatments that involves using hormone medication to stimulate the growth of eggs in the ovaries, removing the eggs and fertilising them with sperm, a lowing them to mature for a few days, then transferring the most promising embryos to the uterus
in vitro fertilisation (IVF)
82