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Human Genetics
The study of inheritance patterns in humans
Cell
Basic structural and functional unit of all known living organisms
Chromosome
A thread-like structure of nucleic acids and protein found in the nucleus of most living cells, carrying genetic information in the form of genes.
DNA
Deoxyribonucleic acid, a self-replicating material present in nearly all living organisms as the main constituent of chromosomes. It is the carrier of genetic information.
Gene
A unit of heredity that is transferred from a parent to offspring and is held to determine some characteristic of the offspring.
Karyotype
A diagram that shows a cell’s chromosomes arranged in order from largest to smallest
Use of Karyotypes
Can be used to determine whether or not an individual has any chromosomal abnormalities
Klinefelter's Syndrome
A male with an XXY chromosome makeup.
Patau's Syndrome
Genetic disorder where a person has three copies of chromosome 13.
Edwards' Syndrome
A genetic disorder caused by the presence of all or part of an extra 18th chromosome.