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Connection

Debopam Samanta to Noonan Syndrome

This is a "connection" page, showing publications Debopam Samanta has written about Noonan Syndrome.

 
Connection Strength
  
 
 
0.517
  
  1. Samanta D. Severe developmental delay and complete agenesis of corpus callosum in a Noonan syndrome patient with SOS1 mutation. Acta Neurol Belg. 2016 Jun; 116(2):223-4.
    View in: PubMed
    Score: 0.517
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.