Term
|
Definition
| an individual who is heterozygous with one normal allele and one recessive allele |
|
|
Term
|
Definition
| a gene located on a sex chromosome (most likely X) resulting in a distinct pattern of inheritance |
|
|
Term
|
Definition
| genes located close enough together on a chromosome that they tend to be inherited together |
|
|
Term
|
Definition
| A genetic disease caused by a sex-linked recessive allele resulting in the lost of one or more blood clotting proteins |
|
|
Term
|
Definition
| a condition where you are missing or have a few extra chromosomes |
|
|
Term
|
Definition
|
|
Term
|
Definition
| a condition where an organism has 3 copies of a chromosome instead of the usual 2 |
|
|
Term
|
Definition
| A condition where an organism has more than 2 sets of chromosomes |
|
|
Term
|
Definition
| A genetic disease caused by the presence of an extra chromosome 21 |
|
|
Term
|
Definition
| a condition where a male child has an extra X chromosome |
|
|
Term
|
Definition
| a condition where a female child is missing an X chromosome |
|
|
Term
|
Definition
| a condition where a male child has an extra Y chromosome |
|
|
