WK1 Chapter 2 Genetics & Prenatal Dev Flashcards
sausage-shaped structure in the nucleus of
cels, containing genes, which are paired,
except in reproductive cels
chromosome
the human body contain —– chromosomes in —–
pairs, with one chromosome in each pair inherited from the mother
and the other inherited from the father
46, 23 pairs
DNA
(deoxyribonucleic acid)
long strand of cel material that stores and
transfers genetic information in a l life forms
segment of DNA containing coded
instructions for the growth and functioning of
the organism
gene
entire store of an organism’s hereditary
information
genome
What would the genome of a female and a males 23rd pair of chromosones be
Male: XY
Female: XX
be XY rather than XXif you were born with a
genotype that included exceptional musical ability, this talent might
never be developed if
your environment provided no access to
musical instruments or musical instruction.
organism’s unique genetic inheritance
genotype
organism’s actual characteristics, derived
from its genotype
phenotype
on a pair of chromosomes, each of two forms
of a gene
allele
alleleRecessive genes are expressed in the phenotype only
when
they are paired with another recessive gene
——– - ——— ———- 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
dominant–recessive inheritance
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
dominant–recessive inheritance
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
incomplete dominance
polygenic inheritance
expression of phenotypic characteristics due
to the interaction of multiple genes
polygenic inheritance
chromosomes that determine whether an
organism is male (XY) or female (XX)
sex chromosomes
eggs in the mother contain an —– chromosome but
sperm may carry —– chromosome
X
either an X or a Y
males more vulnerable than females to a variety of recessive
disorders that are linked to the — ————-
X chromosome
Why can a woman be a carrier of a disorder to the next generation but will not have the disorder herself.
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.
Whay are men more vulnerable to X chromosome linked disorders?
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
pattern of inheritance in which a recessive
characteristic is expressed because it is
carried on the male’s X chromosome
X-linked inheritance
Because of X-linked inheritance, males are at greater risk of
a
wide variety of genetically based conditions, including learning disabilities and intellectual disability
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
behaviour genetics
twins who developed from a single ova and
sperm, and therefore have exactly the same
genotype; also called identical twins
monozygotic (MZ) twins