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Review Question - QID 206507

Fragile X Syndrome QID: 206507 (IM.72)
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QID 206507 (Type "206507" in App Search)
An 8-year-old male presents to a geneticist for further workup of a series of developmental delays, learning disabilities, and dysmorphic features. His past medical history is significant for delays in motor development, including sitting without support at 10 months and wa...
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