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Results 1 - 1 of 1 for Chromosome "17q21.31" duplication syndrome
  1. Chromosome 17 
    ... JA, Brunner HG, de Vries BB. A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism. Nat Genet. ... G, Marangi G. Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype. Nat Genet. 2012 ... doi: 10.1038/ng.2257. Citation on PubMed
    https://medlineplus.gov/genetics/chromosome/17 - Genetics