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Compare and contrast the molecular mechanisms leading to FX syndrome and to FSHMD.
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- a) explain why a diagnosis of ASD is not possible in young babies. b) Given the current understanding of the concordance of ASD, if one of the children detected in these data was an identical twin, how certain is that the other twin would also meet the diagnostic criteria for ASD?What is syndrome ? Name three syndromesHow can Cri-du-Chat syndrome diagnosed? what are the impacts of this disease? and how patients can live with the condition?
- what is the diagnosis of Chronic granulomatous disease (CGD) and explain the genetic mechanism involved. *do not plagiarized*From a genetics point of view in simplified terms Breakdown Muscular Dystrophy 1.) Explain the specific genes involved 2.) Explain becker vs. duchenne dystrophies 3.) Explain treatmentsPropose a theoretical way to cure Down syndrome. Explain why it's theoretical and not practical