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laboratory test
- ... pattern of a genetic condition in a family. Laboratory tests, including genetic testing: Molecular, chromosomal, and biochemical genetic ... testing are used to diagnose genetic disorders. Other laboratory tests that measure the levels of certain substances in ...
- ... may require additional information on clinical validity for laboratory tests performed for people living in that state. Test ...
- ... these individuals the condition can be detected by laboratory tests such as newborn screening tests or tests offered ...
- ... the number of joints affected, the results of laboratory tests, and the family history.Systemic juvenile idiopathic arthritis ...
- ... is often diagnosed unexpectedly by x-rays or laboratory tests done for other reasons. People who develop symptoms ...
- ... 3-hydroxybutyryl-CoA, which can be detected with laboratory tests, but do not have the signs and symptoms ...
- ... high in red blood cells when measured by laboratory tests. The subtypes are indistinguishable based on symptoms. More ...
- ... or proteins, depending on the suspected disorder. The laboratory reports the test results in writing to a person's doctor ...
- ... U.S. federal regulatory standards called the Clinical Laboratory Improvement Amendments (CLIA)? Is the test approved by the U.S. Food and Drug ...
- ... of genetic test that was done. A positive test result means that the laboratory found a change in a particular gene, chromosome, ... condition when the person is unaffected. A negative test result means that the laboratory did not find a change that is known ...