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28 Cards in this Set
- Front
- Back
mutation
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sudden change in offspring
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germ cell
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gamete
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somatic
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body cells or autosomes
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deletion
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mutation where segment of DNA breaks off
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inversion
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mutation where chromosome piece breaks off and attaches in reverse direction
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translocation
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mutation where chromosome piece breaks off and reattaches to a different chromosome
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nondisjunction
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failure of a chromosome to seperate from its homologue in meiosis
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point mutation
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substitution, addition or removal of a nucleotide
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frameshift mutation
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mutation that results in teh misreading of the code during translation because of a change in the reading frame
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autosomes
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body cells
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sex chromosomes
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gametes
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pedigree studies
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study of family history
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carrier
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person who passes on disorder
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genetic screening
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1. blood tests
2. ultrasound 3. amniocentesis 4. sampling chorionic villi |
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genetic counseling
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getting help with disorders
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ultrasound
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method to detect disorders
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amniocentesis
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detcts abnormal amounts of fluids
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sex linked traits
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disorders carried on the sex chromomsomes
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sex influenced traits
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traits influenced by presence of male or female sex hormosomes
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down syndrome
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trisomy 21, extra 21st chromosome
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huntintons disease
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dominant allele, involuntary movements, mental retardation, and death shows up 20s,30s,40s
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Klinefelter syndrom
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extra X, XXY in males, sterile, retarded
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Tay Sachs
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Jewish of East Europe, accumulation of fat deposits
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cystic fibrosis
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caucasians, thick mucus causes breathing and digestion problems
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codey's anemia
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italian
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spina bifida
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spinal cord doesn't from properly
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turner's syndrome
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one X but no 2nd chromosome in females
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disorders inherited by...
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1.single gene pairs
2. X linked genes 3. Groups of gene pairs 4. Extra or missing chromosomes |