Connection

Kenton Holden to Chromosome Deletion

This is a "connection" page, showing publications Kenton Holden has written about Chromosome Deletion.
Connection Strength

0.847
  1. Unbalanced translocation involving partial trisomy 9p and partial monosomy yq with neurodevelopmental delays. J Child Neurol. 2013 Apr; 28(4):524-6.
    View in: PubMed
    Score: 0.394
  2. A deletion in the long arm of chromosome 18 in a child with serum carnosinase deficiency. Pediatr Res. 1997 Feb; 41(2):210-3.
    View in: PubMed
    Score: 0.135
  3. Deletion of 16q24.1 supports a role for the ATP2C2 gene in specific language impairment. J Child Neurol. 2015 Mar; 30(4):517-21.
    View in: PubMed
    Score: 0.115
  4. Acquired microcephaly in blepharophimosis-ptosis-epicanthus inversus syndrome because of an interstitial 3q22.3q23 deletion. Pediatr Neurol. 2014 Jun; 50(6):636-9.
    View in: PubMed
    Score: 0.110
  5. Microdeletion at 4q21.3 is associated with intellectual disability, dysmorphic facies, hypotonia, and short stature. Am J Med Genet A. 2011 Sep; 155A(9):2146-53.
    View in: PubMed
    Score: 0.093
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.