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Fragile X Syndrome: Experiences and Importance of Diagnosis

Fragile X syndrome is an inherited genetic condition, which is most commonly associated with developmental delay and intellectual disability. It affects about one in 4,000 males and about one in 6-8000 females. Clinically, it presents in quite a wide range. Women are almost always less affected than men. Most men will have some form of […]

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What Is Genetic Testing? Understanding the Process and Its Results

Genetic testing can tell us a whole host of information. It can tell us about predispositions to developing cancers. It can tell us about predispositions to developing cardiac disease neurologic disease. It’s oftentimes used as explanations for why there is developmental delay in a child for instance. So we can get a lot of information […]

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Incorporating Medical Genomics into Clinical Practice

medical genomics incorporating 21st century medicine into your clinical practice medical genomics the use of an individual's genetic information as part of their clinical care is based on 150 years of research and innovation observations of the common people and led Austrian monk Gregor Mendel to discover the fundamental principles of genetics and heredity his […]

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