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Results 1 - 3 of 3 for "17q21.31" microdeletion syndrome
  1. Koolen-de Vries syndrome 
    ... Koolen-de Vries syndrome. 17q21.31 deletion syndrome 17q21.31 microdeletion syndrome Chromosome 17q21.31 microdeletion syndrome KANSL1-related intellectual ...
    https://medlineplus.gov/genetics/condition/koolen-de-vries-syndrome - Genetics
  2. Chromosome 17 
    ... in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome. Nat Genet. 2012 Apr 29;44(6):639- ... Brunner HG, de Vries BB. A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism. Nat Genet. ...
    https://medlineplus.gov/genetics/chromosome/17 - Genetics
  3. KANSL1 gene 
    ... JA, Eichler EE. Resolving the breakpoints of the 17q21.31 microdeletion syndrome with next-generation sequencing. Am J Hum Genet. ... in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome. Nat Genet. 2012 Apr 29;44(6):639- ...
    https://medlineplus.gov/genetics/gene/kansl1 - Genetics