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Journal Abstract Search

272 related items for PubMed ID: 8267375

  • 1. Stickler syndrome: report of four cases.
    Kulkarni ML, Sureshkumar C, George VG.
    Ann Dent; 1993; 52(2):23-7. PubMed ID: 8267375
    [No Abstract] [Full Text] [Related]

  • 2. Prenatal diagnosis of Pierre-Robin sequence as part of Stickler syndrome.
    Soulier M, Sigaudy S, Chau C, Philip N.
    Prenat Diagn; 2002 Jul; 22(7):567-8. PubMed ID: 12124689
    [Abstract] [Full Text] [Related]

  • 3. [On the causal and morphological etiology of the Pierre Robin syndrome].
    Becker R, Palm D.
    Dtsch Zahnarztl Z; 1966 Nov 01; 21(11):1321-38. PubMed ID: 5223982
    [No Abstract] [Full Text] [Related]

  • 4. [Stickler syndrome].
    Alvarez de Santos M, Coronado-Monroy A, Medinilla-Vázquez MG, González-Quiroga G, Ramírez-del Río JL, García-Cervantes ML.
    Bol Med Hosp Infant Mex; 1986 Apr 01; 43(4):250-5. PubMed ID: 3707710
    [No Abstract] [Full Text] [Related]

  • 5. The Stickler syndrome (hereditary arthro-ophthalmopathy).
    Say B, Berry J, Barber N.
    Clin Genet; 1977 Sep 01; 12(3):179-82. PubMed ID: 409578
    [Abstract] [Full Text] [Related]

  • 6. Short case presentation. Pierre-Robin sequence.
    Dinwiddie R.
    Paediatr Respir Rev; 2004 Mar 01; 5(1):90, 92. PubMed ID: 15230265
    [No Abstract] [Full Text] [Related]

  • 7. A genetic follow-up study of 64 patients with the Pierre Robin complex.
    Sheffield LJ, Reiss JA, Strohm K, Gilding M.
    Am J Med Genet; 1987 Sep 01; 28(1):25-36. PubMed ID: 3674115
    [Abstract] [Full Text] [Related]

  • 8. Visual complications of Stickler syndrome in paediatric patients with Robin sequence.
    Huang F, Kuo HK, Hsieh CH, Lai JP, Chen PK.
    J Craniomaxillofac Surg; 2007 Mar 01; 35(2):76-80. PubMed ID: 17442580
    [Abstract] [Full Text] [Related]

  • 9. Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia.
    Melkoniemi M, Koillinen H, Männikkö M, Warman ML, Pihlajamaa T, Kääriäinen H, Rautio J, Hukki J, Stofko JA, Cisneros GJ, Krakow D, Cohn DH, Kere J, Ala-Kokko L.
    Eur J Hum Genet; 2003 Mar 01; 11(3):265-70. PubMed ID: 12673280
    [Abstract] [Full Text] [Related]

  • 10. Catel-Manzke syndrome: two new patients and a critical review of the literature.
    Manzke H, Lehmann K, Klopocki E, Caliebe A.
    Eur J Med Genet; 2008 Mar 01; 51(5):452-65. PubMed ID: 18501694
    [Abstract] [Full Text] [Related]

  • 11. [Glaucoma in P. Robin's syndrome].
    Saraux H, Dhermy P.
    Arch Ophtalmol Rev Gen Ophtalmol; 1968 Dec 01; 28(8):793-800. PubMed ID: 4242333
    [No Abstract] [Full Text] [Related]

  • 12. [Syndromes 15. Robin sequence].
    Remmelink HJ, Bosschaart AN.
    Ned Tijdschr Tandheelkd; 1999 Oct 01; 106(10):369-72. PubMed ID: 11930430
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  • 19. New syndrome in three affected siblings.
    Crane JP, Heise RL.
    Pediatrics; 1981 Aug 01; 68(2):235-7. PubMed ID: 7267231
    [Abstract] [Full Text] [Related]

  • 20. [Genetic studies in Pierre Robin syndrome].
    Jörgensen G, Freund HJ.
    ZWR; 1979 Nov 10; 88(21):958-60. PubMed ID: 294009
    [No Abstract] [Full Text] [Related]

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