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28 Cards in this Set
- Front
- Back
Why didn’t most scientist initially believe that chromosomes were responsible for inheritance? |
Because there we so few chromosomes. They didnt see how they could make millions of different possibilities. |
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Not all traits on a chromosome are linked together because of
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crossing over
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If A and B are linked then the AB and ab the possible genotypes would be a __/__ split of __ and __
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AB ab and 50 50
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If they are unlinked then the genotype breakdown would be
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Ab, AB, aB, ab 25% of each
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___show the relative distance between genes.
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recombination frequency
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The two types of chromosomal abnormalities are based on
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chromosome number and chromosomal structure
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__is a picture of all of the chromosomes a person has
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caryotype
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Chromosomes are numbered based on their
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height
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are actually out of order.
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21 and 22
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1.
in meiosis causes disorders in chromosome number |
nondisjunction
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Define Euploid
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having the correct number of each chromosome. |
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Define Anaploid
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dont have the correct number of each chromosome |
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Define Monosomy
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1 of each chromosome, fail to develop |
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Define Trisomy
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3 of the same chromosome, can live
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Trisomy 13 called
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patosyndrome
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Trisomy 18 called
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edward syndrome
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Trisomy 21 called
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downsyndrome
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Sex chromosome __
cause an incorrect number of chromosome __ to be inherited. |
nondisjunction and x
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Inactive X chromosomes are called
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barr bodies
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Klinefelter Syndrome means a person has what chromosome abnormality? |
2x and one y
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Turner’s Syndrome means a person has what chromosome abnormality? |
Girl only has one x, looks less feminine, reduces fertility.
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Triplo-X means a person has what chromosome abnormality? |
Girl can have 3 x’s. Reduces your fertility. |
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Chromosome duplications occur when
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Duplicates part of the dna that isnt supposed to be there.
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Chromosome deletions occur when
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Removes some of the dna.
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Inversions occur when |
Section of the dna gets flipped. |
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Pericentric inversions are
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includes the centromere
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Paracentric inversions are
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on one side of the centromere
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Translocations are when a
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part of the chromosome goes somewhere else, relocation to a different number chromosome. can be genetic
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