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Journal Abstract Search

134 related items for PubMed ID: 7586655

  • 1. Opitz BBBG syndrome: new family with late-onset, serious complication.
    Schrander J, Schrander-Stumpel C, Berg J, Frias JL.
    Clin Genet; 1995 Aug; 48(2):76-9. PubMed ID: 7586655
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  • 2. BBBG syndrome or Opitz syndrome: new family.
    Verloes A, Le Merrer M, Briard ML.
    Am J Med Genet; 1989 Nov; 34(3):313-6. PubMed ID: 2688419
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  • 3. Posterior scalp defects in Opitz syndrome. Another symptom related to a defect in midline development.
    Fryns JP, Delooz J, van den Berghe H.
    Clin Genet; 1992 Dec; 42(6):314-6. PubMed ID: 1493644
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  • 4. Laryngeal cleft: report of eight patients and a review of the literature.
    Tyler DC.
    Am J Med Genet; 1985 May; 21(1):61-75. PubMed ID: 4003449
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  • 5. The G syndrome/Opitz oculo-genital-laryngeal syndrome/Opitz BBB/G syndrome/Opitz-Frias syndrome.
    Conlon BJ, O'Dwyer T.
    J Laryngol Otol; 1995 Mar; 109(3):244-6. PubMed ID: 7745346
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  • 6. G syndrome: an unusual family.
    Allanson JE.
    Am J Med Genet; 1988 Nov; 31(3):637-42. PubMed ID: 3228142
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  • 7. Phenotypic overlap of the BBB and G syndromes.
    Cordero JF, Holmes LB.
    Am J Med Genet; 1978 Nov; 2(2):145-52. PubMed ID: 263434
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  • 8. G syndrome and its otolaryngologic manifestations.
    Howell L, Smith JD.
    Ann Otol Rhinol Laryngol; 1989 Mar; 98(3):185-90. PubMed ID: 2647017
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  • 10. Apparent Opitz BBBG syndrome with a partial duplication of 5p.
    Leichtman LG, Werner A, Bass WT, Smith D, Brothman AR.
    Am J Med Genet; 1991 Aug 01; 40(2):173-6. PubMed ID: 1897571
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  • 11. Male-to-male transmission of Robinow's syndrome. Its occurrence in association with cleft lip and cleft palate.
    Shprintzen RJ, Goldberg RB, Saenger P, Sidoti EJ.
    Am J Dis Child; 1982 Jul 01; 136(7):594-7. PubMed ID: 7091086
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  • 14. Case of polyhydramnios complicated by Opitz G/BBB syndrome.
    Tajima H, Itoh H, Mochizuki A, Nakamura Y, Kobayashi Y, Hirai K, Suzuki K, Sugihara K, Ohishi A, Ohzeki T, Kanayama N.
    J Obstet Gynaecol Res; 2010 Aug 01; 36(4):876-81. PubMed ID: 20666962
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  • 15. Total laryngotracheal hypoplasia in a case of G syndrome.
    Buckley JG, Hinton AE, Penter G, Farndon PA.
    J Laryngol Otol; 1988 Nov 01; 102(11):1056-9. PubMed ID: 3062116
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  • 16. Multidisciplinary management of Opitz G BBB syndrome.
    Parashar SY, Anderson PJ, Cox TC, McLean N, David DJ.
    Ann Plast Surg; 2005 Oct 01; 55(4):402-7. PubMed ID: 16186708
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  • 18. Recurrence of diaphragmatic agenesis associated with multiple midline defects: evidence for an autosomal gene regulating the midline.
    Bird LM, Newbury RO, Ruiz-Velasco R, Jones MC.
    Am J Med Genet; 1994 Oct 15; 53(1):33-8. PubMed ID: 7802033
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  • 19. Ankyloblepharon filiforme adnatum and imperforate anus: a new family with apparently autosomal dominant inheritance.
    Brøndum-Nielsen K.
    Am J Med Genet; 1993 Sep 01; 47(3):439. PubMed ID: 8135297
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