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Journal Abstract Search

112 related items for PubMed ID: 11073546

  • 1. Familial craniofacial fibrous dysplasia: absence of linkage to GNAS1 and the gene for cherubism.
    Mangion J, Edkins S, Goss AN, Stratton MR, Flanagan AM.
    J Med Genet; 2000 Nov; 37(11):E37. PubMed ID: 11073546
    [No Abstract] [Full Text] [Related]

  • 2. Genetic disorders and bone affecting the craniofacial skeleton.
    Chacon GE, Ugalde CM, Jabero MF.
    Oral Maxillofac Surg Clin North Am; 2007 Nov; 19(4):467-74, v. PubMed ID: 18088898
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  • 3. [Fibrous dysplasia of bone].
    Sone T.
    Nihon Rinsho; 2006 Jun 28; Suppl 2():148-51. PubMed ID: 16817371
    [No Abstract] [Full Text] [Related]

  • 4. Fifteen-year follow-up of a family with inherited craniofacial fibrous dysplasia.
    Pierce AM, Sampson WJ, Wilson DF, Goss AN.
    J Oral Maxillofac Surg; 1996 Jun 28; 54(6):780-8. PubMed ID: 8648488
    [No Abstract] [Full Text] [Related]

  • 5. [Cherubism. Familial fibrious dysplasia of the jaw bones].
    Hoppe W, Spranger J, Hansen HG.
    Arch Kinderheilkd; 1966 Aug 28; 174(3):310-20. PubMed ID: 5993997
    [No Abstract] [Full Text] [Related]

  • 6. [Cherubism. A clinical case].
    Bermudo Añino L, Gomez de la Mata Andres J, Gutierrez Perez JL, Garcia Perla A.
    Rev Esp Estomatol; 1986 Aug 28; 34(1):33-8. PubMed ID: 3461509
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  • 14. A sensitive mutation-specific screening technique for GNAS1 mutations in cases of fibrous dysplasia: the first report of a codon 227 mutation in bone.
    Idowu BD, Al-Adnani M, O'Donnell P, Yu L, Odell E, Diss T, Gale RE, Flanagan AM.
    Histopathology; 2007 May 28; 50(6):691-704. PubMed ID: 17493233
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  • 15. Epsilon subunit gene of F(1)F(0)-ATP synthase (ATP5E) on human chromosome 20q13.2-->q13.3 localizes between D20S171 and GNAS1.
    Gross C, Kussmann S, Hehr A, Hansmann I, Schlote D.
    Cytogenet Cell Genet; 2000 May 28; 91(1-4):105-6. PubMed ID: 11173840
    [No Abstract] [Full Text] [Related]

  • 16. Cherubism in siblings: a case report.
    Ongole R, Pillai RS, Pai KM.
    J Can Dent Assoc; 2003 Mar 28; 69(3):150-4. PubMed ID: 12622878
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