1. Give examples of cytogenetic abnormalities, their nomenclature and their clinical features 2. Explain karyotyping, FISH, array CGH3. List scenarios which warrant cytogenetic testing 4. Explain techniques used to assay single gene disorders5. Explain methods to analyze amino acids, organic acids and acylcarnitines6. Use literature/databases to determine significance of genetic and biochemical abnormalities7. Summarize testing best indicated for chromosomal, single gene or biochemical disorders
How well did you achieve this learning goal in this course?
How useful to you were the lectures?
How useful to you were the readings?
How useful to you was/were the Lab observations ?
How useful to you was/were the Unknown assignments?
Please comment on how well the course helped you to think more critically about each of the lecture topics
What aspect of the course was most useful in facilitating your learning? What additions or changes to the course would have further facilitated your learning?
What advice would you give to future students who are taking the course or considering taking the course?