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Connection

Robert Hufnagel to Amelogenesis Imperfecta

This is a "connection" page, showing publications Robert Hufnagel has written about Amelogenesis Imperfecta.
Connection Strength

0.918
  1. The peroxisomal disorder spectrum and Heimler syndrome: Deep phenotyping and review of the literature. Am J Med Genet C Semin Med Genet. 2020 09; 184(3):618-630.
    View in: PubMed
    Score: 0.740
  2. Expanding the genotypic spectrum of Jalili syndrome: Novel CNNM4 variants and uniparental isodisomy in a north American patient cohort. Am J Med Genet A. 2020 03; 182(3):493-497.
    View in: PubMed
    Score: 0.178

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