Connection

Co-Authors

This is a "connection" page, showing publications co-authored by DARYL SCOTT and LISA EMRICK.
Connection Strength

0.296
  1. Recessive loss-of-function variants in DPH1 identified as the molecular cause in a sibling pair previously diagnosed with Fine-Lubinsky syndrome. Am J Med Genet A. 2024 Aug 21; e63845.
    View in: PubMed
    Score: 0.246
  2. COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay. Am J Hum Genet. 2021 09 02; 108(9):1710-1724.
    View in: PubMed
    Score: 0.050
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.