Connection

IVAN CHINN to Syndrome

This is a "connection" page, showing publications IVAN CHINN has written about Syndrome.
Connection Strength

0.112
  1. A novel case discussion of pediatric lipid transfer protein syndrome. J Allergy Clin Immunol Pract. 2021 10; 9(10):3836-3837.
    View in: PubMed
    Score: 0.037
  2. Heterozygous Truncating Variants in POMP Escape Nonsense-Mediated Decay and Cause a Unique Immune Dysregulatory Syndrome. Am J Hum Genet. 2018 06 07; 102(6):1126-1142.
    View in: PubMed
    Score: 0.030
  3. Destabilized SMC5/6 complex leads to chromosome breakage syndrome with severe lung disease. J Clin Invest. 2016 08 01; 126(8):2881-92.
    View in: PubMed
    Score: 0.027
  4. Reactive lymphoid hyperplasia in association with 22q11.2 deletion syndrome and a BRCA2 mutation. Eur J Med Genet. 2011 Jan-Feb; 54(1):63-6.
    View in: PubMed
    Score: 0.018
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.