Connection

Kenton Holden to Genetic Association Studies

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This is a "connection" page, showing publications Kenton Holden has written about Genetic Association Studies.
Kenton Holden
Connection Strength
0.033
Genetic Association Studies
  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: 0.033
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.