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Journal Abstract Search

334 related items for PubMed ID: 10338003

  • 21. Rates of loss of heterozygosity and mitotic recombination in NF2 schwannomas, sporadic vestibular schwannomas and schwannomatosis schwannomas.
    Hadfield KD, Smith MJ, Urquhart JE, Wallace AJ, Bowers NL, King AT, Rutherford SA, Trump D, Newman WG, Evans DG.
    Oncogene; 2010 Nov 25; 29(47):6216-21. PubMed ID: 20729918
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  • 22. [Neurofibromatosis type 2 (NF2)].
    Araki N, Takeshima H, Saya H.
    Gan To Kagaku Ryoho; 1997 Sep 25; 24(11):1427-31. PubMed ID: 9309136
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  • 23. Analysis of chromosome 22 deletions in neurofibromatosis type 2-related tumors.
    Wolff RK, Frazer KA, Jackler RK, Lanser MJ, Pitts LH, Cox DR.
    Am J Hum Genet; 1992 Sep 25; 51(3):478-85. PubMed ID: 1496981
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  • 24. Germline deletion in a neurofibromatosis type 2 kindred inactivates the NF2 gene and a candidate meningioma locus.
    Sanson M, Marineau C, Desmaze C, Lutchman M, Ruttledge M, Baron C, Narod S, Delattre O, Lenoir G, Thomas G.
    Hum Mol Genet; 1993 Aug 25; 2(8):1215-20. PubMed ID: 8401504
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  • 26. Genetic and epigenetic alteration of the NF2 gene in sporadic meningiomas.
    Lomas J, Bello MJ, Arjona D, Alonso ME, Martinez-Glez V, Lopez-Marin I, Amiñoso C, de Campos JM, Isla A, Vaquero J, Rey JA.
    Genes Chromosomes Cancer; 2005 Mar 25; 42(3):314-9. PubMed ID: 15609345
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  • 30. Mapping the breakpoint of a constitutional translocation on chromosome 22 in a patient with NF2.
    Arai E, Tokino T, Imai T, Inazawa J, Ikeuchi T, Tonomura A, Nakamura Y.
    Genes Chromosomes Cancer; 1993 Apr 25; 6(4):235-8. PubMed ID: 7685627
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  • 31. Frequent mutations of NF2 and allelic loss from chromosome band 22q12 in malignant mesothelioma: evidence for a two-hit mechanism of NF2 inactivation.
    Cheng JQ, Lee WC, Klein MA, Cheng GZ, Jhanwar SC, Testa JR.
    Genes Chromosomes Cancer; 1999 Mar 25; 24(3):238-42. PubMed ID: 10451704
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  • 33. Somatic instability of the NF2 gene in schwannomatosis.
    Kaufman DL, Heinrich BS, Willett C, Perry A, Finseth F, Sobel RA, MacCollin M.
    Arch Neurol; 2003 Sep 25; 60(9):1317-20. PubMed ID: 12975302
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  • 34. Sensitive detection of deletions of one or more exons in the neurofibromatosis type 2 (NF2) gene by multiplexed gene dosage polymerase chain reaction.
    Diebold R, Bartelt-Kirbach B, Evans DG, Kaufmann D, Hanemann CO.
    J Mol Diagn; 2005 Feb 25; 7(1):97-104. PubMed ID: 15681480
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  • 38. Intrafamilial correlation of clinical manifestations in neurofibromatosis 2 (NF2).
    Zhao Y, Kumar RA, Baser ME, Evans DG, Wallace A, Kluwe L, Mautner VF, Parry DM, Rouleau GA, Joe H, Friedman JM.
    Genet Epidemiol; 2002 Oct 25; 23(3):245-59. PubMed ID: 12384977
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  • 39. Neurofibromatosis type 2 appears to be a genetically homogeneous disease.
    Narod SA, Parry DM, Parboosingh J, Lenoir GM, Ruttledge M, Fischer G, Eldridge R, Martuza RL, Frontali M, Haines J.
    Am J Hum Genet; 1992 Sep 25; 51(3):486-96. PubMed ID: 1496982
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  • 40. Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas.
    Ruttledge MH, Sarrazin J, Rangaratnam S, Phelan CM, Twist E, Merel P, Delattre O, Thomas G, Nordenskjöld M, Collins VP.
    Nat Genet; 1994 Feb 25; 6(2):180-4. PubMed ID: 8162072
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