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Journal Abstract Search

158 related items for PubMed ID: 9932584

  • 21. A reappraisal of the CHARGE association.
    Oley CA, Baraitser M, Grant DB.
    J Med Genet; 1988 Mar; 25(3):147-56. PubMed ID: 3351900
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  • 22. Airway management in children with major craniofacial anomalies.
    Sculerati N, Gottlieb MD, Zimbler MS, Chibbaro PD, McCarthy JG.
    Laryngoscope; 1998 Dec; 108(12):1806-12. PubMed ID: 9851495
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  • 24. Choanal atresia and associated anomalies.
    Leclerc JE, Fearon B.
    Int J Pediatr Otorhinolaryngol; 1987 Oct; 13(3):265-72. PubMed ID: 3679682
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  • 29. CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene.
    Jongmans MC, Admiraal RJ, van der Donk KP, Vissers LE, Baas AF, Kapusta L, van Hagen JM, Donnai D, de Ravel TJ, Veltman JA, Geurts van Kessel A, De Vries BB, Brunner HG, Hoefsloot LH, van Ravenswaaij CM.
    J Med Genet; 2006 Apr; 43(4):306-14. PubMed ID: 16155193
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  • 30. The CHARGE association: choanal atresia and multiple congenital anomalies.
    Kaplan LC.
    Otolaryngol Clin North Am; 1989 Jun; 22(3):661-72. PubMed ID: 2498809
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  • 31. Radial aplasia in CHARGE syndrome: a new association.
    Wright EM, O'Connor R, Kerr BA.
    Eur J Med Genet; 2009 Jun; 52(4):239-41. PubMed ID: 19375527
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  • 33. Choanal atresia and its associated anomalies. Further support for the CHARGE Association.
    Kaplan LC.
    Int J Pediatr Otorhinolaryngol; 1985 Mar; 8(3):237-42. PubMed ID: 3997378
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  • 35. [An unusual polymalformation syndrome: "CHARGE association" with unilateral "morning glory syndrome"].
    Risse JF, Guillaume JB, Boissonnot M, Bonneau D.
    Ophtalmologie; 1989 Mar; 3(3):196-8. PubMed ID: 2641109
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  • 39. SNP genotyping to screen for a common deletion in CHARGE syndrome.
    Lalani SR, Safiullah AM, Fernbach SD, Phillips M, Bacino CA, Molinari LM, Glass NL, Towbin JA, Craigen WJ, Belmont JW.
    BMC Med Genet; 2005 Feb 14; 6():8. PubMed ID: 15710038
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  • 40. CHARGE association with choanal atresia and inner ear hypoplasia in a child with a de novo chromosome translocation t(2;7)(p14;q21.11).
    Martin DM, Sheldon S, Gorski JL.
    Am J Med Genet; 2001 Mar 01; 99(2):115-9. PubMed ID: 11241468
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