Connection

STEPHANIE BASKIN to COUP Transcription Factor II

This is a "connection" page, showing publications STEPHANIE BASKIN has written about COUP Transcription Factor II.
  1. Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays. Eur J Hum Genet. 2023 10; 31(10):1117-1124.
    View in: PubMed
    Score: 0.054
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.