Molecular screening for fragile X syndrome in children with unexplained intellectual disability and/or autistic behaviour.
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DOI: 10.3897/folmed.64.e60518
Abstract: INTRODUCTION Fragile X syndrome (FXS, OMIM #300624) is the most common inherited form of intellectual disability and the leading monogenic cause of autism. read more here.
Keywords: intellectual disability; screening fragile; molecular screening; syndrome children ... See more keywords