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J Med Genet. 1989 February; 26(2): 119–126.
PMCID: PMC1015563

Stickler's syndrome.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.
  • STICKLER GB, BELAU PG, FARRELL FJ, JONES JD, PUGH DG, STEINBERG AG, WARD LE. HEREDITARY PROGRESSIVE ARTHRO-OPHTHALMOPATHY. Mayo Clin Proc. 1965 Jun;40:433–455. [PubMed]
  • Opitz JM, France T, Herrmann J, Spranger JW. The Stickler syndrome. N Engl J Med. 1972 Mar 9;286(10):546–547. [PubMed]
  • Baraitser M. Marshall/Stickler syndrome. J Med Genet. 1982 Apr;19(2):139–140. [PMC free article] [PubMed]
  • Liberfarb RM, Hirose T, Holmes LB. The Wagner-Stickler syndrome-a genetic study. Birth Defects Orig Artic Ser. 1979;15(5B):145–154. [PubMed]
  • Winter RM, Baraitser M, Laurence KM, Donnai D, Hall CM. The Weissenbacher-Zweymüller, Stickler, and Marshall syndromes: further evidence for their identity. Am J Med Genet. 1983 Oct;16(2):189–199. [PubMed]
  • Kelly TE, Wells HH, Tuck KB. The Weissenbacher-Zweymüller syndrome: possible neonatal expression of the Stickler syndrome. Am J Med Genet. 1982 Jan;11(1):113–119. [PubMed]
  • Keith CG, Dobbs RH, Shaw DG, Cottrall K. Abnormal facies, myopia, and short stature. Arch Dis Child. 1972 Oct;47(255):787–793. [PMC free article] [PubMed]
  • van Balen AT, Falger EL. Hereditary hyaloideoretinal degeneration and palatoschisis. Arch Ophthalmol. 1970 Feb;83(2):152–162. [PubMed]
  • Liberfarb RM, Goldblatt A. Prevalence of mitral-valve prolapse in the Stickler syndrome. Am J Med Genet. 1986 Jul;24(3):387–392. [PubMed]
  • MARSHALL D. Ectodermal dysplasia; report of kindred with ocular abnormalities and hearing defect. Am J Ophthalmol. 1958 Apr;45(4 Pt 2):143–156. [PubMed]
  • Zellweger H, Smith JK, Grützner P. The Marshall syndrome: report of a new family. J Pediatr. 1974 Jun;84(6):868–871. [PubMed]
  • O'Donnell JJ, Sirkin S, Hall BD. Generalized osseous abnormalities in the Marshall syndrome. Birth Defects Orig Artic Ser. 1976;12(5):299–314. [PubMed]
  • Aymé S, Preus M. The Marshall and Stickler syndromes: objective rejection of lumping. J Med Genet. 1984 Feb;21(1):34–38. [PMC free article] [PubMed]
  • WEISSENBACHER G, ZWEYMUELLER E. GLEICHZEITIGES VORKOMMEN EINES SYNDROMS VON PIERRE ROBIN UND EINER FETALEN CHONDRODYSPLASIE. Monatsschr Kinderheilkd. 1964 Jun;112:315–317. [PubMed]
  • KNIEST W. Zur Abgrenzung der Dysostosis enchondralis von der Chondrodystrophie. Z Kinderheilkd. 1952;70(6):633–640. [PubMed]
  • Cohen MM, Knobloch WH, Gorlin RJ. A dominantly inherited syndrome of hyaloideoretinal degeneration, cleft palate and maxillary hypoplasia (Cervenka syndrome). Birth Defects Orig Artic Ser. 1971 Jun;7(7):83–86. [PubMed]
  • Hall J. Stickler syndrome. Presenting as a syndrome of cleft palate, myopia and blindness inherited as a dominant trait. Birth Defects Orig Artic Ser. 1974;10(8):157–171. [PubMed]
  • Insley J, Astley R. A bone dysplasia with deafness. Br J Radiol. 1974 May;47(557):244–251. [PubMed]
  • Miny P, Lenz W. Autosomal recessive deafness with skeletal dysplasia and facial appearance of Marshall syndrome. Am J Med Genet. 1985 Jun;21(2):317–324. [PubMed]
  • Nance WE, Sweeney A. A recessively inherited chondrodystrophy. Birth Defects Orig Artic Ser. 1970 Oct;6(4):25–27. [PubMed]

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