Connection

Kenton Holden to Gene Deletion

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

0.328
  1. Expansion of the deletion 13q syndrome phenotype: a case report. J Child Neurol. 2007 Sep; 22(9):1124-7.
    View in: PubMed
    Score: 0.270
  2. ATP6AP2 variant impairs CNS development and neuronal survival to cause fulminant neurodegeneration. J Clin Invest. 2019 04 15; 129(5):2145-2162.
    View in: PubMed
    Score: 0.038
  3. Expanding CEP290 mutational spectrum in ciliopathies. Am J Med Genet A. 2009 Oct; 149A(10):2173-80.
    View in: PubMed
    Score: 0.020
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.