Term
|
Definition
|
|
Term
|
Definition
|
|
Term
|
Definition
| trait determined by gene on X or Y |
|
|
Term
|
Definition
| tend to be inherited together |
|
|
Term
|
Definition
| diagram of gene positions |
|
|
Term
|
Definition
| 1% increments in frequency of crossing over |
|
|
Term
|
Definition
|
|
Term
|
Definition
|
|
Term
|
Definition
|
|
Term
|
Definition
|
|
Term
|
Definition
|
|
Term
|
Definition
| mov't of DNA segment to another |
|
|
Term
|
Definition
| failure of HLCS to separate |
|
|
Term
|
Definition
| only 1 nucleotide changes |
|
|
Term
|
Definition
|
|
Term
|
Definition
| mutation that shifts all sequences after -> misreading |
|
|
Term
|
Definition
|
|
Term
|
Definition
| chart showing family trait |
|
|
Term
|
Definition
| has one recessive gene which can result in disease in HL pairs |
|
|
Term
|
Definition
| disease caused by CS mutation |
|
|
Term
|
Definition
| char. influenced by many genes |
|
|
Term
|
Definition
| influenced by genes and enviro't |
|
|
Term
|
Definition
| more than 2 alleles for trait |
|
|
Term
|
Definition
| both genes fully expressed |
|
|
Term
|
Definition
| gene is expressed half & half |
|
|
Term
|
Definition
| influenced by presence of X or Y |
|
|
Term
|
Definition
| disease w/involuntary mov'ts and less mental ability |
|
|
Term
|
Definition
| screen where uterus fluid is taken to determine genes |
|
|
Term
|
Definition
| sample to diagnose fetal genotypes |
|
|
Term
|
Definition
| modifying genes to correct disease or improve genome |
|
|
Term
|
Definition
| analyzing parents' genetic make up to predict children's genotype |
|
|