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Results 1 - 1 of 1 for Chromosome "17p13.3" duplication syndrome
  1. Chromosome 17 
    ... considered distinct because it does not include lissencephaly. 17p13.3 duplication syndrome, also called split-hand/foot malformation with long bone deficiency or SHFLD3, is a chromosomal change in which a small piece of chromosome 17 is abnormally copied in each cell. The ...
    https://medlineplus.gov/genetics/chromosome/17 - Genetics