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Connection

Virginia Willis to Bone Diseases, Developmental

This is a "connection" page, showing publications Virginia Willis has written about Bone Diseases, Developmental.

 
Connection Strength
  
 
 
0.499
  
  1. Samanta D, Willis E. Electroencephalographic findings in KBG syndrome: a child with novel mutation in ANKRD11 gene. Acta Neurol Belg. 2015 Dec; 115(4):779-82.
    View in: PubMed
    Score: 0.499
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.