|Searched for: LC Classification is Medicine -- Pathology -- Theories of disease. Etiology. Pathogenesis -- Heredity. Medical genetics -- Genetic disorders. Human chromosome abnormalities
|Results 1 - 5 of 9
This case study examines genetic diseases. Students will use the example given to understand the rules governing the inheritance of single gene dominant, recessive, and sex-linked disorders and be able to apply them to...
The organization, Birth Defects Research For Children, was founded by the parents of a child who was born with defects due to a medication taken by the mother when she was pregnant. The goals of this organization and...
What is spinal muscular atrophy (SMA)? It is an inherited disease that affects approximately 1 in 10,000 infants born in the United States each year. There are four types of SMA, which can cause the muscles to function...
The Genetic Home Reference, offered through the National Library of Medicine, offers easy-to-understand "consumer information about genetic conditions and the genes responsible for those conditions." The site consists...
The National Human Genome Research Institute (NHGRI) has many accolades to its credit, not the least being their work on sequencing the human genome. They have made substantial contributions to every sector of genomic...
|Search time: 0.824 seconds
Manage your resources
Save, organize, and share resources that you find.
Subscribe to bulletins
Automatically be notified about new resources that match your interests.
It's easy, fast, and FREE!