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Connection

Robert Hufnagel to Bone Diseases, Developmental

This is a "connection" page, showing publications Robert Hufnagel has written about Bone Diseases, Developmental.
Connection Strength

0.204
  1. Homozygous missense variant in BMPR1A resulting in BMPR signaling disruption and syndromic features. Mol Genet Genomic Med. 2019 11; 7(11):e969.
    View in: PubMed
    Score: 0.173
  2. A novel dominant COL11A1 mutation resulting in a severe skeletal dysplasia. Am J Med Genet A. 2014 Oct; 164A(10):2607-12.
    View in: PubMed
    Score: 0.030

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