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PUBMED FOR HANDHELDS

Journal Abstract Search

190 related items for PubMed ID: 21605101

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  • 2. Identification of DKC1 gene mutations in Japanese patients with X-linked dyskeratosis congenita.
    Kanegane H, Kasahara Y, Okamura J, Hongo T, Tanaka R, Nomura K, Kojima S, Miyawaki T.
    Br J Haematol; 2005 May; 129(3):432-4. PubMed ID: 15842668
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  • 4. Missense mutation in a patient with X-linked dyskeratosis congenita.
    Kraemer DM, Goebeler M.
    Haematologica; 2003 Apr; 88(4):ECR11. PubMed ID: 12681984
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  • 8. Dyskeratosis congenita--two siblings with a new missense mutation in the DKC1 gene.
    Coelho JD, Lestre S, Kay T, Lopes MJ, Fiadeiro T, Apetato M.
    Pediatr Dermatol; 2011 Apr; 28(4):464-6. PubMed ID: 21736606
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  • 11. Dyskeratosis congenita.
    Handley TP, McCaul JA, Ogden GR.
    Oral Oncol; 2006 Apr; 42(4):331-6. PubMed ID: 16140563
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  • 15. Recurrent A353V mutation in a Thai family with X-linked dyskeratosis congenita.
    Viprakasit V, Tanphaichitr VS.
    Haematologica; 2001 Aug; 86(8):871-2. PubMed ID: 11522545
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  • 16. One novel and two recurrent missense DKC1 mutations in patients with dyskeratosis congenita (DKC).
    Heiss NS, Mégarbané A, Klauck SM, Kreuz FR, Makhoul E, Majewski F, Poustka A.
    Genet Couns; 2001 Aug; 12(2):129-36. PubMed ID: 11491307
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  • 17. [Dyskeratosis congenita in a 40-year-old patient].
    Benoit S, Kraemer D, Bröcker EB, Goebeler M.
    Hautarzt; 2006 Apr; 57(4):313-5. PubMed ID: 15789197
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  • 19. DKC1 gene mutation in a Taiwanese kindred with X-linked dyskeratosis congenita.
    Lin JH, Lee JY, Tsao CJ, Chao SC.
    Kaohsiung J Med Sci; 2002 Nov; 18(11):573-7. PubMed ID: 12513020
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