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Biochemistry pp 247-287 | Cite as

Medical Genetics

  • Sara L. Tobin
Part of the Oklahoma Notes book series (OKLAHOMA)

Abstract

Medical genetics involves the study of chromosomal DNA abnormalities that cause genetic diseases, such as mutations or misdistribution of chromosomes. DNA sequences vary among individuals, accounting for our individuality in appearance, personal biochemistry, resistance to disease, and response to medication. Deleterious mutations are more serious than these individual variations and result in the appearance of disease symptoms in affected family members. We will review the patterns of genetic inheritance, recombinant DNA techniques, and the use of molecular genetics to predict whether or not individuals or their children may inherit a genetic disease.

Keywords

Cystic Fibrosis Restriction Fragment Length Polymorphism Normal Gene Huntington Disease Coat Color 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer-Verlag New York, Inc. 1995

Authors and Affiliations

  • Sara L. Tobin

There are no affiliations available

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