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Results 1 - 2 of 2 for "Koolen-de" varies syndrome
  1. Chromosome 17 
    ... a variety of physical abnormalities.Most people with Koolen-de Vries syndrome are missing a sequence of about 500,000 base pairs, also written as 500 kilobases (kb), at position q21.31 on chromosome 17. The exact size of the deletion varies among affected individuals, but it contains at least ...
    https://medlineplus.gov/genetics/chromosome/17 - Genetics
  2. Koolen-de Vries syndrome 
    ... gene to be nonfunctional.The microdeletion that causes Koolen-de Vries syndrome occurs on the long (q) arm of chromosome 17 at a location designated q21.31. While the exact size of the deletion varies among affected individuals, most are missing a sequence ...
    https://medlineplus.gov/genetics/condition/koolen-de-vries-syndrome - Genetics