Connection

Kenton Holden to Fragile X Syndrome

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This is a "connection" page, showing publications Kenton Holden has written about Fragile X Syndrome.
Kenton Holden
Connection Strength
0.381
Fragile X Syndrome
  1. Severe Hunter syndrome (mucopolysaccharidosis II) phenotype secondary to large deletion in the X chromosome encompassing IDS, FMR1, and AFF2 (FMR2). J Child Neurol. 2012 Jun; 27(6):786-90.
    View in: PubMed
    Score: 0.381
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.