Chapter 13 Vocabulary

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20 Terms

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aneuploid

individual with an error in chromosome number; includes chromosome segment deletions and duplications

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autosome

any of the non-sex chromosomes

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centimorgan (cM)

(also, map unit) relative distance that corresponds to a 0,01 recombination frequency

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Chromosomal Theory of Inheritance

theory proposing that chromosomes are the genes' vehicles and that their behavior during meiosis is the physical basis of the inheritance patterns that Mendel observed

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chromosome inversion

detachment, 180° rotation, and chromosome arm reinsertion

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euploid

individual with the appropriate number of chromosomes for their species

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homologous recombination

process by which homologous chromosomes undergo reciprocal physical exchanges at their arms, also crossing over

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karyogram

a karyotype's photographic image

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karyotype

an individual's chromosome number and appearance; includes the size, banding patterns, and centromere position

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monosomy

otherwise diploid genotype in which one chromosome is missing

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nondisjunction

failure of synapsed homologs to completely separate and migrate to separate poles during the meiosis' first cell division

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nonparental (recombinant) type

progeny resulting from homologous recombination that exhibits a different allele combination compared with its parents

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paracentric

inversion that occurs outside the centromere

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parental types

progeny that exhibits the same allelic combination as its parents

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pericentric

inversion that involves the centromere

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polyploid

individual with an incorrect number of chromosome sets

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recombination frequency

average number of crossovers between two alleles; observed as the number of nonparental types in a progeny's population

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translocation

process by which one chromosome segment dissociates and reattaches to a different, nonhomologous chromosome

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trisomy

otherwise diploid genotype in which one entire chromosome duplicates

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X inactivation

condensing X chromosomes into Barr bodies during embryonic development in females to compensate for the double genetic dose