The Role of Genetics in Rare Diseases: Understanding Fragile X Syndrome | Science 37
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YouTubeScience 37
The Role of Genetics in Rare Diseases: Understanding Fragile X Syndrome | Science 37
Many children with Fragile X show signs of developmental delay by age 1 or 2, but the condition is often not diagnosed until later. Delays in speech, poor eye contact, sensitivity to sound, and behavioral problems are often early clues—but without genetic testing, they may be misattributed to general developmental disabilities or other ...
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