Term
|
Definition
Condition of having multiple sets of chromosomes derived from two or more different species. |
|
|
Term
|
Definition
Condition in which the chromosome number differs from the wild type by part of a chromosome set. |
|
|
Term
|
Definition
Condition of having multiple sets of chromosomes all derived from a single species. |
|
|
Term
|
Definition
An inherited large-scale change in chromosome structure or number. |
|
|
Term
|
Definition
Mutation in which one or more base pairs is absent. |
|
|
Term
|
Definition
Presence of one or more extra copies of a chromosomal region. |
|
|
Term
|
Definition
A chromosomal rearrangement involving removal of a segment, its rotation through 180 degrees, and its reinsertion in the same location. |
|
|
Term
|
Definition
The set of chromosomes within a cell sorted into pairs and arranged from large to small. |
|
|
Term
|
Definition
Failure of homologous chromosomes or sister chromatids to segregate at meiosis or mitosis. |
|
|
Term
|
Definition
Condition of having more than two sets of chromosomes. |
|
|
Term
|
Definition
Exchange of parts between nonhomologous chromosomes. |
|
|