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