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Original Article

The Weissenbacher-Zweymüller phenotype in the neonatal period as an expression in the continuum of manifestations of the hereditary arthroophthalmopathies

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Pages 159-163 | Accepted 15 May 1987, Published online: 08 Jul 2009

References

  • Herrmann J. The Stickler syndrome (hereditary arthro-ophthalmopathy. Birth Def. Orig. Art. Ser. 1975; 11/2: 76–103
  • Kelly Th. The Weissenbacher-Zweymiiller syndrome: Possible neonatal expression of the Stickler syndrome. Amer. J. med. Gen. 1983; 11: 113–119
  • O'donnell J. J. Generalized osseous abnormalities in the Marshall syndrome. Birth Def. 1976; 12/5: 239–314
  • Stickler G. B., et al. Hereditary progressive arthro-ophthalmopathy. Mayo Clin. Proc. 1965; 40: 433–455
  • Wagner H. Ein bisher unbekanntes Erbleiden des Auges (Degeneratio hyaloideo-retinalis hereditaria), beobachtet im Kan-ton Zurich). Klin. Mbl. Augenheilk. 1938; 100: 840–857
  • Weissenbacher G., Zweymüller E. Gleichzeitiges Vorkommen eines Syndroms von Pierro Robin und einer feta-len Chondrodysplasie. Mschr. Kinderheilk. 1964; 112: 315–317
  • Winter R. M., et al. The Weissenbacher-Zweymiiller and Marshall syndromes: Further evidence for their identity. Amer. J. med. Gen. 1983; 16: 189–199

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