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Journal Abstract Search

267 related items for PubMed ID: 8986284

  • 41. Branchio-oto-renal dysplasia and branchio-oto dysplasia: report of eight new cases.
    Martini A, Comacchio F, Candiani F, Vio S.
    Am J Otol; 1987 Mar; 8(2):116-22. PubMed ID: 3591918
    [Abstract] [Full Text] [Related]

  • 42. [Malformation processes in the middle ear. Branchio-oto-renal syndrome (BOR)].
    Motta G, Mesolella M, Salafia M.
    Acta Otorhinolaryngol Ital; 1996 Apr; 16(2 Suppl 53):42-6. PubMed ID: 8928671
    [Abstract] [Full Text] [Related]

  • 43. Tricho-rhino-phalangeal and branchio-oto syndromes in a family with an inherited rearrangement of chromosome 8q.
    Haan EA, Hull YJ, White S, Cockington R, Charlton P, Callen DF.
    Am J Med Genet; 1989 Apr; 32(4):490-4. PubMed ID: 2773990
    [Abstract] [Full Text] [Related]

  • 44. [Inheritance on commissural lip pits].
    Zervou-Valvi F, Bazopoulou-Kyrkanidou E.
    Odontostomatol Proodos; 1988 Oct; 42(5):363-9. PubMed ID: 3152608
    [Abstract] [Full Text] [Related]

  • 45. Frequency of the branchio-oto-renal (BOR) syndrome in children with profound hearing loss.
    Fraser FC, Sproule JR, Halal F.
    Am J Med Genet; 1980 Oct; 7(3):341-9. PubMed ID: 7468659
    [Abstract] [Full Text] [Related]

  • 46. PHAVER syndrome: an autosomal recessive syndrome of limb pterygia, congenital heart anomalies, vertebral defects, ear anomalies, and radial defects.
    Powell CM, Chandra RS, Saal HM.
    Am J Med Genet; 1993 Nov 01; 47(6):807-11. PubMed ID: 8279476
    [Abstract] [Full Text] [Related]

  • 47. The branchio-oto-renal (BOR) syndrome: report of bilateral renal agenesis in three sibs.
    Carmi R, Binshtock M, Abeliovich D, Bar-Ziv J.
    Am J Med Genet; 1983 Apr 01; 14(4):625-7. PubMed ID: 6846397
    [Abstract] [Full Text] [Related]

  • 48. Branchiootic syndrome--a clinical case report and review of the literature.
    Amer I, Falzon A, Choudhury N, Ghufoor K.
    J Pediatr Surg; 2012 Aug 01; 47(8):1604-6. PubMed ID: 22901925
    [Abstract] [Full Text] [Related]

  • 49. Preauricular sinus, nephrolithiasis, infantine eczema and natal tooth: a new association.
    Yılmaz AE, Sarıfakıoglu E, Aydemır S, Taş T, Orün E, Aydemır H.
    Eur J Dermatol; 2011 Aug 01; 21(2):234-7. PubMed ID: 21398203
    [Abstract] [Full Text] [Related]

  • 50. Hereditary congenital cholesteatoma. A variant of branchio-oto dysplasia.
    Lipkin AF, Coker NJ, Jenkins HA.
    Arch Otolaryngol Head Neck Surg; 1986 Oct 01; 112(10):1097-100. PubMed ID: 3755982
    [Abstract] [Full Text] [Related]

  • 51. Syndromic ear anomalies and renal ultrasounds.
    Wang RY, Earl DL, Ruder RO, Graham JM.
    Pediatrics; 2001 Aug 01; 108(2):E32. PubMed ID: 11483842
    [Abstract] [Full Text] [Related]

  • 52. Branchio-oto-renal dysplasia associated with tetralogy of Fallot.
    Daggilas A, Antoniades K, Palasis S, Aidonis A.
    Head Neck; 1992 Aug 01; 14(2):139-42. PubMed ID: 1601651
    [Abstract] [Full Text] [Related]

  • 53. X-linked syndrome of branchial arch and other defects.
    Toriello HV, Higgins JV, Abrahamson J, Waterman DF, Moore WD.
    Am J Med Genet; 1985 May 01; 21(1):137-42. PubMed ID: 4039890
    [Abstract] [Full Text] [Related]

  • 54. Branchio-oto-renal syndrome: reduced penetrance and variable expressivity in four generations of a large kindred.
    Rollnick BR, Kaye CI.
    Am J Med Genet; 1987 May 01; 27(1):233. PubMed ID: 3605200
    [No Abstract] [Full Text] [Related]

  • 55. The earpits-deafness syndrome. Clinical and genetic aspects.
    Cremers CW, Fikkers-Van Noord M.
    Int J Pediatr Otorhinolaryngol; 1980 Nov 01; 2(4):309-22. PubMed ID: 6964893
    [Abstract] [Full Text] [Related]

  • 56. Stickler and branchio-oto-renal syndromes in a patient with mutations in EYA1 and COL2A1 genes.
    Olavarrieta L, Morales-Angulo C, del Castillo I, Moreno F, Moreno-Pelayo MA.
    Clin Genet; 2008 Mar 01; 73(3):262-7. PubMed ID: 18177466
    [Abstract] [Full Text] [Related]

  • 57. A new type of maxillofacial dysostosis, inherited as an X-linked or autosomal recessive trait.
    Ensink RJ, Brunner HG, Cremers CW.
    Genet Couns; 1997 Mar 01; 8(4):285-90. PubMed ID: 9457496
    [Abstract] [Full Text] [Related]

  • 58. Hemifacial microsomia and the branchio-oto-renal syndrome.
    Rollnick BR, Kaye CI.
    J Craniofac Genet Dev Biol Suppl; 1985 Mar 01; 1():287-95. PubMed ID: 3877103
    [Abstract] [Full Text] [Related]

  • 59. [Bilateral anotia associated with a tracheo-esophageal fistula, ectopic pancreas, vertebro-costal anomalies and anal imperforation. A new malformative syndrome?].
    Vignola G.
    Pathologica; 1973 Mar 01; 65(941):167-71. PubMed ID: 4786850
    [No Abstract] [Full Text] [Related]

  • 60. Patient with an EYA1 mutation with features of branchio-oto-renal and oto-facio-cervical syndrome.
    Mercer C, Gilbert R, Loughlin S, Foulds N.
    Clin Dysmorphol; 2006 Oct 01; 15(4):211-212. PubMed ID: 16957474
    [No Abstract] [Full Text] [Related]

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