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Journal Abstract Search

236 related items for PubMed ID: 144680

  • 21. Mitral valve prolapse in a patient with frontometaphyseal dysplasia.
    Park JM, Contreras EA, Garcia RR.
    Clin Pediatr (Phila); 1986 Sep; 25(9):469-71. PubMed ID: 3742931
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  • 22. Skeletal alterations in Edwards' disease (trisomy 18 syndrome).
    Franceschini P, Fabris C, Ponzone A, Bogetti G, Grassi E, Randaccio M.
    Ann Radiol (Paris); 1974 Sep; 17(4):361-7. PubMed ID: 4447310
    [No Abstract] [Full Text] [Related]

  • 23. Skeletal dysplasia syndrome with progeroid appearance, characteristic facial and limb anomalies, multiple synostoses, and distinct skeletal changes: a variant example of the Lenz-Majewski syndrome.
    Chrzanowska KH, Fryns JP, Krajewska-Walasek M, Van den Berghe H, Wisniewski L.
    Am J Med Genet; 1989 Apr; 32(4):470-4. PubMed ID: 2773987
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  • 26. Radiographic manifestations of the arthrogryposis syndrome.
    Poznanski AK, La Rowe PC.
    Radiology; 1970 May; 95(2):353-8. PubMed ID: 5439444
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  • 28. Congenital distal humeral dysplasia: a case report.
    Joseph B, Varghese RA.
    Pediatr Radiol; 2003 Jan; 33(1):7-10. PubMed ID: 12497228
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  • 30. Radiological changes of frontometaphyseal dysplasia in the neonate.
    Nishimura G, Takano H, Aihara T, Ohashi H, Fukushima Y, Satoh M.
    Pediatr Radiol; 1995 Nov; 25 Suppl 1():S143-6. PubMed ID: 8577509
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  • 31. Frontometaphyseal dysplasia: a progressive disease of bone and connective tissue.
    Danks DM, Mayne V.
    Birth Defects Orig Artic Ser; 1974 Nov; 10(12):57-60. PubMed ID: 4282264
    [No Abstract] [Full Text] [Related]

  • 32. Interstitial deletion of a chromosome 7 (q11.2q22.1) in a child with splithand/splitfoot malformation.
    Pfeiffer RA.
    Ann Genet; 1984 Nov; 27(1):45-8. PubMed ID: 6609672
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  • 33. [Case of craniometaphyseal dysplasia considered to be typical in x-ray figures].
    Katsumata N, Tanabe M, Aono K, Morino Y, Watanabe S.
    Rinsho Hoshasen; 1971 Aug; 16(8):637-42. PubMed ID: 5209368
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  • 37. Asymmetric and symmetric long bone bowing in two sibs: an apparently new bone dysplasia.
    Moore LA, Moore CA, Smith JA, Weaver DD.
    Am J Med Genet; 1993 Nov 15; 47(7):1072-7. PubMed ID: 8291526
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