- aneuploid
 - individual with an error in chromosome number; includes deletions and duplications of chromosome segments
 
- autosome
 - any of the non-sex chromosomes
 
- centimorgan (cM)
 - (also, map unit) relative distance that corresponds to a recombination frequency of 0.01
 
- Chromosomal Theory of Inheritance
 - theory proposing that chromosomes are the vehicles of genes and that their behavior during meiosis is the physical basis of the inheritance patterns that Mendel observed
 
- chromosome inversion
 - detachment, 180° rotation, and reinsertion of a chromosome arm
 
- euploid
 - individual with the appropriate number of chromosomes for their species
 
- homologous recombination
 - process by which homologous chromosomes undergo reciprocal physical exchanges at their arms, also known as crossing over
 
- karyogram
 - photographic image of a karyotype
 
- karyotype
 - number and appearance of an individuals chromosomes; includes the size, banding patterns, and centromere position
 
- monosomy
 - otherwise diploid genotype in which one chromosome is missing
 
- nondisjunction
 - failure of synapsed homologs to completely separate and migrate to separate poles during the first cell division of meiosis
 
- nonparental (recombinant) type
 - progeny resulting from homologous recombination that exhibits a different allele combination compared with its parents
 
- paracentric
 - inversion that occurs outside of the centromere
 
- parental types
 - progeny that exhibits the same allelic combination as its parents
 
- pericentric
 - inversion that involves the centromere
 
- polyploid
 - individual with an incorrect number of chromosome sets
 
- recombination frequency
 - average number of crossovers between two alleles; observed as the number of nonparental types in a population of progeny
 
- translocation
 - process by which one segment of a chromosome dissociates and reattaches to a different, nonhomologous chromosome
 
- trisomy
 - otherwise diploid genotype in which one entire chromosome is duplicated
 
- X inactivation
 - condensation of X chromosomes into Barr bodies during embryonic development in females to compensate for the double genetic dose