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Journal Abstract Search

322 related items for PubMed ID: 12566519

  • 1. Molecular study of frequency of mosaicism in neurofibromatosis 2 patients with bilateral vestibular schwannomas.
    Kluwe L, Mautner V, Heinrich B, Dezube R, Jacoby LB, Friedrich RE, MacCollin M.
    J Med Genet; 2003 Feb; 40(2):109-14. PubMed ID: 12566519
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  • 2. Molecular genetic analysis of the NF2 gene in young patients with unilateral vestibular schwannomas.
    Mohyuddin A, Neary WJ, Wallace A, Wu CL, Purcell S, Reid H, Ramsden RT, Read A, Black G, Evans DG.
    J Med Genet; 2002 May; 39(5):315-22. PubMed ID: 12011146
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  • 3. Bilateral vestibular schwannomas in older patients: NF2 or chance?
    Evans DG, Freeman S, Gokhale C, Wallace A, Lloyd SK, Axon P, Ward CL, Rutherford S, King A, Huson SM, Ramsden RT, Manchester NF2 service.
    J Med Genet; 2015 Jun; 52(6):422-4. PubMed ID: 25725045
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  • 8. Mutations of the neurofibromatosis type 2 gene and lack of the gene product in vestibular schwannomas.
    Sainz J, Huynh DP, Figueroa K, Ragge NK, Baser ME, Pulst SM.
    Hum Mol Genet; 1994 Jun; 3(6):885-91. PubMed ID: 7951231
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  • 11. [Neurofibromatosis type 2 (central neurofibromatosis or bilateral acoustic neuromas, vestibular schwannomas): from phenotype to gene].
    Sabol Z, Kipke-Sabol L, Miklić P, Hajnsek-Propadalo S, Sabol F.
    Lijec Vjesn; 2006 Jun; 128(9-10):309-16. PubMed ID: 17128670
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  • 12. Mutations and allelic loss of the NF2 gene in neurofibromatosis 2-associated skin tumors.
    Kluwe L, Friedrich RE, Hagel C, Lindenau M, Mautner VF.
    J Invest Dermatol; 2000 May; 114(5):1017-21. PubMed ID: 10771486
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  • 13. Mosaicism in sporadic neurofibromatosis 2 patients.
    Kluwe L, Mautner VF.
    Hum Mol Genet; 1998 Dec; 7(13):2051-5. PubMed ID: 9817921
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  • 14. Clinical manifestations of mutations in the neurofibromatosis type 2 gene in vestibular schwannomas (acoustic neuromas).
    Welling DB.
    Laryngoscope; 1998 Feb; 108(2):178-89. PubMed ID: 9473065
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  • 15. NF2 genetic alterations in sporadic vestibular schwannomas: clinical implications.
    Lassaletta L, Torres-Martín M, Peña-Granero C, Roda JM, Santa-Cruz-Ruiz S, Castresana JS, Gavilan J, Rey JA.
    Otol Neurotol; 2013 Sep; 34(7):1355-61. PubMed ID: 23921927
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  • 19. The neurofibromatosis type 2 gene is inactivated in schwannomas.
    Twist EC, Ruttledge MH, Rousseau M, Sanson M, Papi L, Merel P, Delattre O, Thomas G, Rouleau GA.
    Hum Mol Genet; 1994 Jan; 3(1):147-51. PubMed ID: 8162016
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  • 20. A murine model of neurofibromatosis type 2 that accurately phenocopies human schwannoma formation.
    Gehlhausen JR, Park SJ, Hickox AE, Shew M, Staser K, Rhodes SD, Menon K, Lajiness JD, Mwanthi M, Yang X, Yuan J, Territo P, Hutchins G, Nalepa G, Yang FC, Conway SJ, Heinz MG, Stemmer-Rachamimov A, Yates CW, Wade Clapp D.
    Hum Mol Genet; 2015 Jan 01; 24(1):1-8. PubMed ID: 25113746
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