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Connection

Mark Hoffman to Genetic Diseases, Inborn

This is a "connection" page, showing publications Mark Hoffman has written about Genetic Diseases, Inborn.

 
Connection Strength
  
 
 
0.154
  
  1. Fowler SA, Saunders CJ, Hoffman MA. Variation among Consent Forms for Clinical Whole Exome Sequencing. J Genet Couns. 2018 02; 27(1):104-114.
    View in: PubMed
    Score: 0.154
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.