Connection

Kenton Holden to Exome

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This is a "connection" page, showing publications Kenton Holden has written about Exome.
Kenton Holden
Connection Strength
0.034
Exome
  1. A novel familial autosomal dominant mutation in ARID1B causing neurodevelopmental delays, short stature, and dysmorphic features. Am J Med Genet A. 2016 12; 170(12):3313-3318.
    View in: PubMed
    Score: 0.034
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.