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Connection

Kathleen Sullivan to Hyperostosis, Cortical, Congenital

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This is a "connection" page, showing publications Kathleen Sullivan has written about Hyperostosis, Cortical, Congenital.
Kathleen Sullivan
Connection Strength
0.232
Hyperostosis, Cortical, Congenital
  1. Li D, Mailand N, Ewing E, Hoffmann S, Caswell RC, Pang L, Eason J, Dou Y, Sullivan KE, Hakonarson H, Levine MA. Quantitative hypermorphic FAM111A alleles cause autosomal recessive Kenny-Caffey syndrome type 2 and osteocraniostenosis. JCI Insight. 2025 Mar 24; 10(6).
    View in: PubMed
    Score: 0.232
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.
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