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This Cystic Fibrosis: A DNA Case Study lesson plan also includes:
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- Genetic Structure Probe—Cystic Fibrosis A DNA Case Study, Spanish (.docx)
- Student Handout 1—Cystic Fibrosis A DNA Case Study, English (.pdf)
- Student Handout 1—Cystic Fibrosis A DNA Case Study, English (.docx)
- Student Handout 1—Cystic Fibrosis A DNA Case Study, Spanish (.pdf)
- Student Handout 2—Cystic Fibrosis A DNA Case Study, English (.pdf)
- Student Handout 2—Cystic Fibrosis A DNA Case Study, English (.docx)
- Student Handout 2—Cystic Fibrosis A DNA Case Study, Spanish (.pdf)
- Student Handout 3—Cystic Fibrosis A DNA Case Study, English (.pdf)
- Student Handout 3—Cystic Fibrosis A DNA Case Study, English (.docx)
- Student Handout 3—Cystic Fibrosis A DNA Case Study, Spanish (.pdf)
- Student Handout 4—Cystic Fibrosis A DNA Case Study (.pdf)
- Student Handout 4—Cystic Fibrosis A DNA Case Study (.docx)
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Around six percent of babies are born with serious genetic disorders. Young scientists learn more about what causes these disorders and the effect they have. They begin with a case study of cystic fibrosis before expanding to research other disorders to better understand genetics.
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CCSS:
Adaptable
NGSS:
Designed
Concepts
Additional Tags
Instructional Ideas
- Have a student with cystic fibrosis or a parent or other member of the community speak to the class
- Invite a doctor in to talk about the importance of early detection and newborn screenings for genetic disorders
Classroom Considerations
- Relies on prior knowledge of DNA and chromosome replication
Pros
- Includes clear instructions for you and the pupils
- Provides ways to combine reading and researching with movement
- Offers opportunities for both individual and group work
Cons
- None