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Journal Abstract Search

161 related items for PubMed ID: 8882795

  • 1. Opitz GBBB syndrome and the 22q11.2 deletion.
    Lacassie Y, Arriaza MI.
    Am J Med Genet; 1996 Mar 29; 62(3):318. PubMed ID: 8882795
    [No Abstract] [Full Text] [Related]

  • 2. Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion.
    McDonald-McGinn DM, Driscoll DA, Bason L, Christensen K, Lynch D, Sullivan K, Canning D, Zavod W, Quinn N, Rome J.
    Am J Med Genet; 1995 Oct 23; 59(1):103-13. PubMed ID: 8849001
    [Abstract] [Full Text] [Related]

  • 3. Opitz G/BBB syndrome: clinical comparisons of families linked to Xp22 and 22q, and a review of the literature.
    Robin NH, Opitz JM, Muenke M.
    Am J Med Genet; 1996 Mar 29; 62(3):305-17. PubMed ID: 8882794
    [No Abstract] [Full Text] [Related]

  • 4. Distal deletion of chromosome 13 in a child with the "opitz" GBBB syndrome.
    Urioste M, Arroyo I, Villa A, Lorda-Sánchez I, Barrio R, López-Cuesta MJ, Rueda J.
    Am J Med Genet; 1995 Oct 23; 59(1):114-22. PubMed ID: 8849002
    [Abstract] [Full Text] [Related]

  • 5. Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion.
    McDonald-McGinn DM, Emanuel BS, Zackai EH.
    Am J Med Genet; 1996 Aug 23; 64(3):525-6. PubMed ID: 8862635
    [No Abstract] [Full Text] [Related]

  • 6. Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2.
    Robin NH, Feldman GJ, Aronson AL, Mitchell HF, Weksberg R, Leonard CO, Burton BK, Josephson KD, Laxová R, Aleck KA, Allanson JE, Guion-Almeida ML, Martin RA, Leichtman LG, Price RA, Opitz JM, Muenke M.
    Nat Genet; 1995 Dec 23; 11(4):459-61. PubMed ID: 7493033
    [Abstract] [Full Text] [Related]

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  • 8. Opitz oculo-genital-laryngeal syndrome (Opitz BBB/G compound syndrome).
    Sedano HO, Gorlin RJ.
    Am J Med Genet; 1988 Jul 23; 30(3):847-9, 851. PubMed ID: 3189406
    [No Abstract] [Full Text] [Related]

  • 9. Naguib-Richieri-Costa syndrome: hypertelorism, hypospadias, and polysyndactyly syndrome.
    Teebi AS.
    Am J Med Genet; 1992 Sep 01; 44(1):115-7. PubMed ID: 1325738
    [No Abstract] [Full Text] [Related]

  • 10. Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 36-2004. A 23-day-old infant with hypospadias and failure to thrive.
    Stoler JM, Leach NT, Donahoe PK.
    N Engl J Med; 2004 Nov 25; 351(22):2319-26. PubMed ID: 15564548
    [No Abstract] [Full Text] [Related]

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  • 12. Laryngeal manifestations in Opitz BBB/G syndrome.
    Arcand P, Abela A, Al-Ammar A, Quintal MC.
    J Otolaryngol; 2000 Jun 25; 29(3):179-82. PubMed ID: 10883834
    [No Abstract] [Full Text] [Related]

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  • 14. The hypertelorism-hypospadias (BBB) syndrome in members of two families.
    Horák I, Smahel Z.
    Acta Chir Plast; 1987 Jun 25; 29(2):61-76. PubMed ID: 2444051
    [No Abstract] [Full Text] [Related]

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  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17. A practical application of fluorescent in situ hybridization to the Wolf-Hirschhorn syndrome.
    Fagan K, Colley P, Partington M.
    Pediatrics; 1994 May 01; 93(5):826-7. PubMed ID: 8165089
    [No Abstract] [Full Text] [Related]

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  • 19. The Philadelphia story: the 22q11.2 deletion: report on 250 patients.
    McDonald-McGinn DM, Kirschner R, Goldmuntz E, Sullivan K, Eicher P, Gerdes M, Moss E, Solot C, Wang P, Jacobs I, Handler S, Knightly C, Heher K, Wilson M, Ming JE, Grace K, Driscoll D, Pasquariello P, Randall P, Larossa D, Emanuel BS, Zackai EH.
    Genet Couns; 1999 May 01; 10(1):11-24. PubMed ID: 10191425
    [Abstract] [Full Text] [Related]

  • 20. BBBG syndrome or Opitz syndrome: new family.
    Verloes A, Le Merrer M, Briard ML.
    Am J Med Genet; 1989 Nov 01; 34(3):313-6. PubMed ID: 2688419
    [Abstract] [Full Text] [Related]

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