Connection

Kenton Holden to Transcription Factors

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

0.144
  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: 0.098
  2. A novel in-frame deletion in ARX is associated with lissencephaly with absent corpus callosum and hypoplastic genitalia. Am J Med Genet A. 2005 Sep 15; 138(1):70-2.
    View in: PubMed
    Score: 0.046
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.