A | B |
chromosome | tightly coiled lengths of DNA wrapped around protein cores |
karyotype | a set of chromosomes in which the homologous pairs are matched and arranged by size |
diploid | a cell that contains 2 sets of chromosomes |
haploid | a cell which contains a single set of chromosomes |
sex chromosomes | chromosomes that determine the sex of an organism, in humans the 23d pair |
human female | XX |
human male | XY |
mitosis | eukaryotic cell division |
cytokinesis | cellular division at the end of mitosis |
cell cycle | life span of a cell including growth and division |
tumor | clump of cells growing where they should not be |
cancer | uncontrolled cell division and growth |
mutation | change in the genetic code |
gamete | egg or sperm, a haploid reproductive cell |
meiosis | cellular division that produces gametes |
crossing over | the exchange of genetic information between homologous chromosomes |
Interphase | The phase that cells are in for the majority of their life |
Prophase | The phase where chromosomes get short and thick and the nuclear membrane breaks down |
Metaphase | The chromosomes pair up near the equator of the cell |
Anaphase | The chromosome pairs split and migrate toward opposite ends of the cell |
Telophase | Chromosomes get longer and thinner while a new nuclear membrane forms |
Binary Fission | When reproduction occurs by splitting in two |
Cytokinesis | The old cell divides into two new, but smaller cells |
Gene | A segment of a chromosome that has information for one trait |
Centromere | This holds two identical chromosomes together temporarily |
Homologous Chromosomes | The two chromosomes of a pair |
Zygote | A fertilized egg |
Autosomes | Chromosomes that are not the sex chromosomes |
CVS | Sampling cells from the villi in the chorion (birth defect test) |
Polydactyly | Having extra fingers or toes |
Deletion | Mutation where some DNA is left out |
Duplication | Mutation where some DNA is in a chromosome more than one place |
Inversion | Mutation where the DNA order is reversed for part of the DNA |
Translocation | Mutation where some of the DNA is found at the wrong place on a chromosome |
Nondisjunction | When a chromosome pair does not separate when it is supposed to |
Trisomy | Nondisjunction which results in an extra chromosome |
Down's Syndrome | Results from an extra 21st chromosome |
Turner's SYndrome | Results from a missing sex chromosome |
Sex Chromosomes | X and Y |
Klinefelter's Syndrome | Results from XXY for sex chromosomes |
Oogenesis | Formation of egg cells |
Spermatogenesis | Formation of sperm |
DNA | Deoxyribonucleic acid |
# of Chromosomes in most human cells | 46 |
# of chromosomes in human gametes | 23 |
Gametes contain | 22 autosomes and 1 sex chromosome |
Synthesis Phase | DNA is duplicated |
G1 & G2 Phases | Growth |
Given to determine if a baby has a birth defect | Blood Test |
Age of which parent increases risk of Down's Syndrome | Mother |
Sex-Linked Trait (Bleeder's Disease) | Hemophilia |
Drugs | Leading cause of Birth Defects |
Amniocentesis | Testing the amniotic fluid for potential birth defects |
These individuals are sterile, but may look mostly female | Turner's Syndrome |
Color Blindness | Sex-linked |
Atrophy | Means muscles get smaller |
Muscular Dystrophy | Disease where the muscles wither away |