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Section .2.
| Question | Answer |
|---|---|
| pedigree | a diagram that shows the occurrence of a genetic trait in several generations of a family |
| carrier | an inactive substance that is a vehicle for a radioactive tracer of the same substance and that assists in its recovery after some chemical reaction |
| genetic disorder | an abnormal condition that a person inherits through genes or chromosomes |
| polygenic | of or relating to an inheritable character that is controlled by several genes at once |
| complex character | characters that are influenced strongly both by the environment and by genes |
| multiple allele | genes with three or more alleles |
| codominance | situation in which both alleles of a gene contribute to the phenotype of the organism |
| incomplete dominance | one allele is not completely dominant over the other allele |
| sex-influenced trait | an autosomal trait that is influenced by the presence of male or female sex hormones |
| Huntington's disease | human genetic disease caused by a dominant allele; characterized by uncontrollable body movements and degeneration of the nervous system; usually fatal 10 to 20 years after the onset of symptoms. |
| amniocentesis | technique that allows a physician to remove from the amnion |
| chorionic villi sampling | sampling of cells derived from the zygote that grow between the mother's uterus and placenta between the 8th and 10th week of pregnancy |
| genetic counseling | guidance for prospective parents on the likelihood of genetic disorders in their future children |
| gene therapy | The insertion of working copies of a gene into the cells of a person with a genetic disorder in an attempt to correct the disorder |