The 16p11.2 region is both sides by bands segmental duplications, short strings of nearly identical DNA to the loss to the loss, shuffling or flanking amplification of this region during genetic recombination purchase dapoxetine online . Many human diseases by these types of chromosomal rearrangements caused, but this is the first recurrent microdeletion in autism. Too small to be seen under a microscope, said Christian.
The most common known genetic cause of autism, linked to about one to three % of cases is a much larger duplication of part of chromosome 15, with about a dozen. Gene the chromosome 15 abnormality with autism and intellectual disability () connected to the chromosome 16 deletion is, however not consistently associated with intellectual disability.
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