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PUBMED FOR HANDHELDS

Journal Abstract Search

227 related items for PubMed ID: 12887821

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  • 3. [Characteristics of gene structure in facioscapulohumeral muscular dystrophy-related 4q35 subtelomere and genotype-phenotype correlation in Chinese Han population].
    Wang ZQ, Wu ZY, Wang N, Lin MT, Murong SX.
    Zhonghua Yi Xue Za Zhi; 2009 Feb 10; 89(5):304-9. PubMed ID: 19563705
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  • 5. A new dosage test for subtelomeric 4;10 translocations improves conventional diagnosis of facioscapulohumeral muscular dystrophy (FSHD).
    van der Maarel SM, Deidda G, Lemmers RJ, Bakker E, van der Wielen MJ, Sandkuijl L, Hewitt JE, Padberg GW, Frants RR.
    J Med Genet; 1999 Nov 10; 36(11):823-8. PubMed ID: 10544225
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  • 6. The Facioscapulohumeral muscular dystrophy region on 4qter and the homologous locus on 10qter evolved independently under different evolutionary pressure.
    Rossi M, Ricci E, Colantoni L, Galluzzi G, Frusciante R, Tonali PA, Felicetti L.
    BMC Med Genet; 2007 Mar 02; 8():8. PubMed ID: 17335567
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  • 7. [Gene diagnosis of facioscapulohumeral muscular dystrophy].
    Zhang JL, Shen DG, Zhou PK, Liu JW, Jia N, Liu H, Wang HB, Yang SX, Frants RR.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Jun 02; 20(3):232-4. PubMed ID: 12778451
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  • 16. Molecular combing reveals allelic combinations in facioscapulohumeral dystrophy.
    Nguyen K, Walrafen P, Bernard R, Attarian S, Chaix C, Vovan C, Renard E, Dufrane N, Pouget J, Vannier A, Bensimon A, Lévy N.
    Ann Neurol; 2011 Oct 02; 70(4):627-33. PubMed ID: 22028222
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  • 17. Typical facioscapulohumeral dystrophy phenotype in patients without FSHD 4q35 deletion.
    Krasnianski M, Neudecker S, Eger K, Jakubiczka S, Zierz S.
    J Neurol; 2003 Sep 02; 250(9):1084-7. PubMed ID: 14504970
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  • 20. Methylation of the FSHD syndrome-linked subtelomeric repeat in normal and FSHD cell cultures and tissues.
    Tsien F, Sun B, Hopkins NE, Vedanarayanan V, Figlewicz D, Winokur S, Ehrlich M.
    Mol Genet Metab; 2001 Nov 02; 74(3):322-31. PubMed ID: 11708861
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