| Term | Definition |
|
Karyotype |
photograph of chromosomes grouped in orders in pairs |
|
Sex Chromosomes |
one of 2 chromosomes that determine an individuals sex |
|
Autosomes |
chromosomes that are not a sex chromosome |
|
Pedigree |
chart that shows the relationships within a family |
|
Nondisjunction |
error in meiosis in which homologous chromosomes fail to seperate |
|
Sex Linked Gene |
gene located on the X or Y chromosome; mainly found on the X chromosome |
|
Blood Types |
A= IAIA or IAi; B= IBIB or IBi; AB=IAIB; O= ii |
|
Sickle Cell Anemia |
a small change in the DNA of a single gene that affects the structure of a protein |
|
Cystic Fibrosis |
a small change in the DNA of a single gene that affects the structure of a protein |
|
Hemophilia |
a protein necessary for normal blood clotting is missing |
|
Duchenne Muscular Dystrophy |
caused by a defective version of the gene that codes for a muscle protein |
|
Color Blindness |
human genes associated with color vision is located on the X chromsome; in males a defective version of any one of these genes produces colorblindness |
|
Down Syndrome |
an individual born with 3 copies of a chromosome |
|
Klinefelter's |
in males; extra X chromosome that interferes with meiosis and usually prevents the individual from reproducing |
|
Turners |
in females; usually inherits only one X chromosome |