Chapter 2 - Genetic Bases of Childhood Development Flashcards

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1
Q

Why do relatively few genetic disorders involve dominant alleles?

A

inherited disorders are rarely carried by dominant alleles because individuals with such a disorder usually don’t live long enough to have children

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2
Q

alleles

A

a variation of a specific gene

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3
Q

Define: sickle-cell trait

A

disorder in which individuals show signs of mild anemia only when they are seriously deprived of oxygen; occurs in individuals who have one dominant allele for normal blood cells and one recessive sickle-cell allele

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4
Q

Define: sex chromosomes

A

the 23rd pair of chromosomes; these determine the sex of the child

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5
Q

Define: recessive

A

an allele whose instructions are ignored when it is combined with a dominant allele

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6
Q

Define: polygenic inheritance

A

when phenotypes are the result of the combined activity of many separate genes

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7
Q

Define: phenotype

A

the physical, behavioural, and psychological features that are the result of the interaction between one’s genes and the environment

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8
Q

Define: niche-picking

A

the process of deliberately seeking environments that are compatible with one’s genetic makeup

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9
Q

Define: autosomes

A

the first 22 pairs of chromosomes, the chromosomes in each pair are about the same size

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10
Q

Define: behavioural genetics

A

the branch of genetics that deals with inheritance of behavioral and psychological traits

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11
Q

Define: chromosomes

A

tiny structures in the nucleus that contain genetic material

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12
Q

Define: deoxyribonucleic acid—DNA

A

a molecule composed of four nucleotide bases; the biochemical basis of heredity.

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13
Q

Define: dizygotic twins

A

twins from two separate eggs fertilized by two separate sperm, genetically, fraternal twins are just like any other siblings, on average, about half their genes are the same

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14
Q

Define: dominant

A

the form of an allele whose chemical instructions are followed

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15
Q

Define/explain: Trisomy 21 aka Down Syndrome

A

a genetic disorder that is caused by an extra 21st chromosome

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16
Q

Define: epigenesis

A

continuous interplay between genes and multiple levels of the environment (from cells to culture) that drives development

17
Q

Define: gene

A

a group of nucleotide bases that provide a specific set of biochemical instructions

18
Q

Define: genotype

A

the complete set of genes that makes up a person’s heredity

19
Q

Define: monozygotic twins

A

identical twins, come from a single fertilized egg that split in two, have identical genes

20
Q

Define: incomplete dominance

A

the situation in which one allele does not dominate another completely

21
Q

Define/explain: in vitro fertilization

A

mixing sperm and egg together in a laboratory dish and then placing several fertilized eggs in a woman’s uterus

22
Q

Define: heritability coefficient

A

the extent to which differences between people reflect heredity

23
Q

Define: homozygous

A

a person who inherits the same allele on a pair of chromosomes, the biochemical instructions on the allele are followed

24
Q

Define: Huntington’s disease

A

a type of dementia caused by a dominant allele; characterized by degeneration of the nervous system

25
Q

Define: heterozygous

A

a person who inherits different alleles, the instructions of the dominant allele are followed, those of the recessive allele are ignored

26
Q

Define: nonshared environmental influences

A

forces within a family that make children different from one another

27
Q

What fraction of attempts at in vitro fertilization succeed?

A

only about one-third of the attempts at in vitro fertilization succeed

28
Q

How many sperm are contained in a teaspoon of ejaculate?

A

from 200 million to 500 million sperm

29
Q

A child’s 46 chromosomes include approximately how many thousand genes?

A

a child’s 46 chromosomes include about 25,000 genes, chromosome 1 has the most genes (nearly 3,000) and the Y chromosome has the fewest (just over 200)