Heredity and Disease 유전과질병 유정병
- 최초 등록일
- 2013.05.25
- 최종 저작일
- 2013.05
- 48페이지/ MS 파워포인트
- 가격 3,000원
목차
1. Learning Objectives
2. DNA, Genes and chromosome
3. Mitosis
4. Mendelian inheritance
5. Genetic Counseling
6. Diagnosis of Genetic Diseases
7. Hereditary Diseases
8. Autosomal Dominant Diseases
9. Polydactyly
10. Achondroplasia
11. Marfan syndrome
12. Familial hypercholesterolemia
13. Autosomal Recessive Diseases
14. Phenylketonuria
15. Neonatal heel prick
16. Galactosemia
17. Sickle cell anemia
18. Tay-Sachs disease
19. Albinism
20. Sex-Linked Inheritance
21. Color blindness
22. Hemophilia
23. Fragile X Syndrome
24. Familial disease
25. Abnormal Chromosome Diseases
26. Down Syndrome
27. Cri du chat syndrome
28. Turner syndrome
29. Klinefelter syndrome
30. Hermaphrodite
31. Congenital disease VS hereditary disease
32. Gene Therapy
본문내용
After studying this chapter, you should be able to
-Describe DNA’s unique composition and its role in heredity
-Describe mechanisms of transmission of hereditary diseases and give examples
-Explain genetic diseases based on abnormal chromosome construction
-Describe genetic diseases involving anomalies and numbers in the sex chromosomes
-Compare and contrast congenital diseases and hereditary disorders
-Discuss the concept of gene therapy
DNA, Genes and chromosome
*DNA (deoxyribonucleic acid)
- double helix which is made of four chemical bases (ATGC)
- DNA replication
: during cell division for the growth and development
: during reproduction of organism (at meiosis)
*Gene
- a locatable regions of genomic sequence, corresponding to a unit of inheritance
- holds the information to build and maintain a living organism (gene expression)
참고 자료
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