Genetic evaluation and counseling involves a consultation that provides an individual's risk of acquiring inheritable conditions. Learn more about this service.
Whole genome sequencing allows doctors to closely analyze a patient's genes for mutations and health indicators. Learn about this procedure.
Pregnant and expecting mothers have the opportunity to learn a lot about their unborn child's health with today's screening and diagnostic tests.
A hereditary cancer syndrome is an inherited syndrome in which there is an increased risk of developing cancer.
Mosaicism is a condition that occurs when a person has two or more genetically separate sets of cells in his or her body.
Molecular diagnostics involves analyzing DNA or RNA for red flags that can pinpoint the potential emergence of a specific disease.
With advancements in non-invasive imaging and surgical techniques, it is now possible to treat many problems in a fetus before birth.
Gaucher disease is a rare, inherited disorder that causes fatty substances to build up in the spleen, liver and other organs.
Whole exome sequencing is a type of genetic sequencing performed from blood or saliva samples. Learn about this procedure.
Angelman Syndrome is a rare genetic disorder affects the nervous system. People with the condition may have developmental delays, learning disabilities, speech impairment and problems with balance and coordination.