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In this final section of the AP Biology unit on Heredity, we’ll take a look at chromosomal inheritance and how it influences the heredity of genetic diseases. We’ll start reviewing chromosomal inheritance. Then, we’ll see how different genetic disorders can be caused both by mutations in specific genes and nondisjunction events that lead to genomes with too many or too few chromosomes. In this section, we’ll also review how to read a pedigree. We’ll see several common pedigree examples and learn about some different clues that can help us identify which type of inheritance pattern is at play (autosomal dominant, autosomal recessive, sex-linked, etc.). Finally, we’ll see specific examples of how nondisjunction events can cause genetic disorders in humans, and how they sometimes lead to speciation events in other populations of animals. Resources related to this Video: ● Overview: The same information, for those who prefer to read. Get it here: https://biologydictionary.net/ap-biol... ● Quick Test Prep: You can find answers to the questions in this video here: https://biologydictionary.net/ap-biol... ● PowerPoint: If you like our presentation, you can download the file here: https://biologydictionary.net/ap-biol... ● Crossword Puzzle: Need to brush up on your vocabulary for this section? Get a crossword (with answers) here: https://biologydictionary.net/ap-biol... All of our individual resources for this subject are free to view, and only $0.99 to download! Enjoy!