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22 Cards in this Set

  • Front
  • Back
allele
alternative form a gene - alleles occur at the same locus on homologous chromosomes
autosome
any chromosome other than the sex-determining pair
Barr body
dark-staining body in the nuclei of female mammals that contains condensed, inactive X chromosome
crossing-over
exchange of segments between nonsister chromatids of a tetrad during meiosis
diploid (2n) number
cell condition in which two of each type of chromosome are present
Down syndrome
is trisomy 21; an individual has 3 copies of chromosome 21; most cases, the egg contained 2 copies
dyad
chromosome composed of two sister chromatids
haploid (n) number
cell condition in which only 1 of each type of chromosome is present
homologous chromosome
member of a pair of chromosomes that are alike and come together in synapsis during prophase of the first meiotic division; a homolgue
homologue
member of a pair of chromosomes that are alike and come together in synapsis during prophase of the first meiotic division; a homologous chromosome
interkinesis
period of time between meiosis I and meiosis II during which no DNA replication takes place
Klinefelter syndrome
condition caused by the inheritance of XXY chromosomes
life cycle
recurring pattern of genetically programmed events by which individuals grow, develop, maintain themselves, and reproduce
meiosis, meiosis I, meiosis II
type of nuclear division that occurs as part of sexual reproduction in which the daughter cells receive the haploid number of chromosomes in varied combinations
nondisjunction
failure of homologous chromosomes or daughter chromosomes to separate during meiosis I and meiosis II, respectively
oogenesis
production of eggs in females by the process of meiosis and maturation
sex chromosome
chromosome that determines the sex of an individual; in humans, females have two X chromosomes, and males have an X and a Y chromosome
spermatogenesis
production of sperm in males by the process of meiosis and maturation
synapsis
pairing of homolgous chromosomes during meiosis I
tetrad
homologous chromosomes, each having sister chromatids that are joined during meiosis; also called bivalent
Turner syndrome
condition caused by the inheritcance of a single X chromosome
zygote
diploid cell formed by the union of two gametes; the product of fertilization