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37 Cards in this Set
- Front
- Back
Chromosomes |
Rod like structures called chromosomes which store and transmit genetic information |
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Chromosomes are made of what |
Are made up of a chemical substance called DNA |
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Gene |
Is a segment of DNA along the length of a chromosome |
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Protein-coding genes |
Which directly affect our bodies characteristics, lie along the human chromosomes |
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Regulator genes |
Modify the instructions given by protein coding genes, greatly complicating their genetic impact |
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Gametes |
Sex cells- the sperm and ovum- combine |
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Autosomes |
22 of the 23 pairs of chromosomes are matching pairs called Autosomes. The 23rd pair consists of sex chromosomes. |
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Female chromosomes |
Pair is called XX |
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Male chromosomes |
Pair called XY |
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Fraternal or dizygotic twins |
The most common type of multiple offspring, resulting from the release and fertilization of two ova |
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Meiosis |
Gametes are formed through a cell division process called meiosis, which halves the number of chromosomes normally present in body cells. When sperm and ovum unite at conception, the resulting cell called is a zygote |
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Allele |
Forming of a gene |
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Homozygous |
If the alleles from both parents are alike the child is homozygous. And will display the inherited trait. |
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Heterozygous |
If the alleles differ, then the child is heterozygous, and relationships between the allele influence the phenotype |
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Dominant- recessive inheritance |
In many heterozygous pairings dominant recessive inheritance occurs: only one allele affect the child characteristics. It is called dominant; the second allele, which has no effect, is called recessive |
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Carriers |
Heterozygous individuals with just one recessive allele (Db) can pass that trait to their children. Therefore they are called carriers of the trait |
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Identical or monozygotic twins |
A zygote that has started to duplicate separates into two clusters of cells that develop into two individuals called identical twins because they have the same genetic makeup |
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Incomplete dominance |
A pattern of inheritance in which both alleles are expressed in the phenotype, resulting in a combined trait, or one that is intermediate between the two |
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X linked inheritance |
When a harmful allele is carried on the X chromosome, x-linked inheritance applies. Males are more likely to be affected because their sex chromosomes do not match |
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Mutation |
a sudden but permanent change in a segment of DNA |
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Genomic imprinting |
Alleles are imprinted, or chemically marked through regulatory processes Within the genome, in such a way that one pair member either mothers or the father's it activated, regardless of its makeup |
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Polygenic inheritance |
In which meaning genes affect the characteristic in question |
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Genetic counseling |
Is a communication process designed to help couples access their chances of giving birth to a baby with a hereditary disorder and choose the best course of action interview of risks and family goals |
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Prenatal diagnostic methods |
Medical procedures that permit detection of developmental problems before birth |
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Coparenting |
Mutually supporting each other's parenting behaviors |
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Socioeconomic status |
Research access a family's standing on this continuum through an index called socioeconomic status (SES), which combines three related, but not completely overlapping variables: 1) years of education 2) the prestige of one's job and the skill it requires, both of which measure social status 3) income which measures economic status |
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Subcultures |
Groups of people with beliefs and customs that differ from those of the larger culture |
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Extended family households |
In which parent and child live with one or more adult relatives |
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Public policies |
Laws and government programs designed to improve current conditions |
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Behavioral genetics |
Is a field devoted to uncovering the contributions of nature and nurture to this diversity in human traits and abilities |
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Heritability estimates |
Measure the extent to which individual differences in complex traits in a specific population are due too genetic factors |
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Kinship studies |
Which compare the characteristics of family members |
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Gene- environment interaction |
Means that because of their genetic makeup, individuals differ in their responsiveness to qualities of the environment |
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Gene- environment correlation |
Our genes influence the environments to which we are exposed |
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Niche-picking |
This tendency to actively choose environments that compliment our heredity |
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Epigenesis |
Which means development resulting from ongoing, bi-directional exchanges between heredity and all levels of the environment |
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Methylation |
A biochemical process triggered by certain experiences, in which a set of chemical compounds lands on top of a gene and changes its impact, reducing or silencing its expression |