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Biol 104 Ch. 12

Campbell Biology in Focus Ch. 12

TermDefinition
Genetic map a list of the genetic loci along a chromosome
Linkage map a genetic map based on recombination frequencies in homologous chromosomes
Deletion the loss of a chromosome fragment which leads to missing genes
Duplication a broken fragment of a chromosome becomes reattached to a sister or non-sister chromatid
Inversion chromosomal fragment breaks off and then is reattached, but in reverse orientation
Translocation a broken chromosome fragment attaches to a non homologous chromosome
Linked genes genes close enough together on the same chromosomes that they are inherited together.
Wild type the phenotype for the trait most commonly observed in natural populations
Sex linked genes genes located on either the x or the y chromosome
Barr body the inactivated x chromosome and each cell of a female mammal.
Parental types offspring whose phenotypes match their parents
Non-disjunction homologous chromosomes or sister chromatids fail to separate during meiosis. This results in an incorrect chromosome number in gamete cells.
Aneuploidy general term for a zygote that has an abnormal number of a particular chromosome
Monosomic a zygote that is missing one, of a set of two chromosomes
Trisomic a zygote that has three of a particular chromosome
Polyploidy organisms that have more than two complete chromosome sets in all somatic cells
Created by: PRO Teacher etucci
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