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    Donna J. Eteson, BA, DMD

    TitleAdjunct Assistant Professor of Clinical
    SchoolHerman Ostrow School of Dentistry of USC
    DepartmentDentistry
    AddressCHL 2nd Floor
    Off Campus
    Los Angeles California 90089-0641
    Phone+1 323 669 2130
    vCardDownload vCard

      Collapse Bibliographic 
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      Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help.
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      1. Lin HJ, Kakkis ED, Eteson D, Lachman RS. DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): a new patient and delineation of neurologic variability among recessive cases. Am J Med Genet. 1993 Sep 15; 47(4):534-9. PMID: 8256819.
        View in: PubMed
      2. Sillence DO, Ritchie HE, Dibbayawan T, Eteson D, Brown K. Fragilitas ossium (fro/fro) in the mouse: a model for a recessively inherited type of osteogenesis imperfecta. Am J Med Genet. 1993 Jan 15; 45(2):276-83. PMID: 8456819.
        View in: PubMed
      3. Rimoin DL, Eteson D, Sillence DO. Comparisons and correlations of skeletal defects in mouse and human. Pathol Immunopathol Res. 1988; 7(1-2):139-45. PMID: 3222202.
        View in: PubMed
      4. Eteson D, Beluffi G, Burgio GR, Belloni C, Lachman RS, Rimoin DL. Pseudodiastrophic dysplasia: a distinct newborn skeletal dysplasia. J Pediatr. 1986 Oct; 109(4):635-41. PMID: 3761077.
        View in: PubMed
      5. Ornoy A, Adomian GE, Eteson D, Burgeson RE, Rimoin DL. The role of mesenchyme-like tissue in the pathogenesis of thanatophoric dysplasia. Am J Med Genet. 1985 Aug; 21(4):613-30. PMID: 4025393.
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      6. Eteson D, Sillence DO, Lachman RS, Rimoin DL. The mouse skeletal mutants: models for the human skeletal dysplasias. Prog Clin Biol Res. 1985; 187:141-51. PMID: 4059229.
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      7. Eteson D, Adomian GE, Ornoy A, Koide T, Sugiura Y, Calabro A, Lungarotti S, Mastroiacovo P, Lachman RS, Rimoin DL. Fibrochondrogenesis: radiologic and histologic studies. Am J Med Genet. 1984 Oct; 19(2):277-90. PMID: 6507479.
        View in: PubMed
      8. Chen H, Immken L, Lachman R, Yang S, Rimoin DL, Rightmire D, Eteson D, Stewart F, Beemer FA, Opitz JM. Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies: delineation of a new entity and review of lethal forms of multiple pterygium syndrome. Am J Med Genet. 1984 Apr; 17(4):809-26. PMID: 6720746.
        View in: PubMed
      9. Eteson D, Stewart RE. Craniofacial defects in the human skeletal dysplasias. Birth Defects Orig Artic Ser. 1984; 20(3):19-45. PMID: 6391575.
        View in: PubMed