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Connection

SARAH ELSEA to Whole Genome Sequencing

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This is a "connection" page, showing publications SARAH ELSEA has written about Whole Genome Sequencing.
SARAH ELSEA
Connection Strength
0.121
Whole Genome Sequencing
  1. Functional analysis of novel DEAF1 variants identified through clinical exome sequencing expands DEAF1-associated neurodevelopmental disorder (DAND) phenotype. Hum Mutat. 2017 12; 38(12):1774-1785.
    View in: PubMed
    Score: 0.121
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.