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Chapter 11 Vocabulary

AB
carrieran individual who is heterozygous for a recessive disorder
pedigreea diagram that traces the inheritance of a particular trait through several generations
cystic fibrosisone of the most common recessive disorders among Caucasians
albinisma disorder resulting in the absence of melanin
Tay-Sachs diseasea disorder on chromosome 15: predominant in Jews of eastern European descent
Huntington's diseasea dominant genetic disorder that affects the central nervous system
achrondroplasiaa dominant disorder: dwarfism
incomplete dominanceneither allele is dominant over the other so the heterozygous phenotype is an intermediate phenotype
codominanceboth alleles are expressed in the heterozygous condition
multiple allelesmore than two alleles: human blood groups
epistasisone allele hides the effects of another
sex chromosomechromosome that determines an individuals gender
autosome22 pairs of chromosomes
sex-linked traittraits controlled by genes on the x chromosome
polygenic traitarise from the interaction of multiple pairs of genes
sickle-cell diseasea blood disease found in people of African descent
dosage compensation/x compensationone X chromosome stops working in each of the female's body cells
Barr bodiesthe inactivated X chromosome that shows up as a darkly stained
hemophiliaa recessive sex-linked disorder that is characterized by delayed clotting of the blood
concordance ratethe percentage of identical twins who both express a given trait
karyotypepairs of homologous chromosomes that are arranged in decreasing size to produce a micrograph
telomereprotective caps on the ends of chromosomes
nondisjunctionan event when sister chromatids fail to separate properly
trisomya set of three chromosomes
monosomyhaving only one particular type of chromosome
Down syndrometrisomy 21
Red-green colored blindnessa recessive sex-linked trait affects about 8% of males in the U.S.


Konawa High School
Konawa, OK

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