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Donna J. Eteson, BA, DMD

Title(s)Adjunct Assistant Professor of Clinical
Phone+1 323 669 2130
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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 DJ, 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.
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    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.
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    3. Rimoin DL, Eteson DJ, Sillence DO. Comparisons and correlations of skeletal defects in mouse and human. Pathol Immunopathol Res. 1988; 7(1-2):139-45. PMID: 3222202.
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    4. Eteson DJ, 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.
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    5. Ornoy A, Adomian GE, Eteson DJ, 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 DJ, 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 DJ, 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.
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    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.
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    9. Eteson DJ, Stewart RE. Craniofacial defects in the human skeletal dysplasias. Birth Defects Orig Artic Ser. 1984; 20(3):19-45. PMID: 6391575.
      View in: PubMed