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Journal Abstract Search

183 related items for PubMed ID: 15239924

  • 1. Genomic analysis of facioscapulohumeral muscular dystrophy.
    Clapp J, Bolland DJ, Hewitt JE.
    Brief Funct Genomic Proteomic; 2003 Oct; 2(3):213-23. PubMed ID: 15239924
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  • 2. Contractions of D4Z4 on 4qB subtelomeres do not cause facioscapulohumeral muscular dystrophy.
    Lemmers RJ, Wohlgemuth M, Frants RR, Padberg GW, Morava E, van der Maarel SM.
    Am J Hum Genet; 2004 Dec; 75(6):1124-30. PubMed ID: 15467981
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  • 3. Distinguishing the 4qA and 4qB variants is essential for the diagnosis of facioscapulohumeral muscular dystrophy in the Chinese population.
    Wang ZQ, Wang N, van der Maarel S, Murong SX, Wu ZY.
    Eur J Hum Genet; 2011 Jan; 19(1):64-9. PubMed ID: 20736973
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  • 4. Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophy.
    Lemmers RJ, Wohlgemuth M, van der Gaag KJ, van der Vliet PJ, van Teijlingen CM, de Knijff P, Padberg GW, Frants RR, van der Maarel SM.
    Am J Hum Genet; 2007 Nov; 81(5):884-94. PubMed ID: 17924332
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  • 5. Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere.
    Lemmers RJ, de Kievit P, Sandkuijl L, Padberg GW, van Ommen GJ, Frants RR, van der Maarel SM.
    Nat Genet; 2002 Oct; 32(2):235-6. PubMed ID: 12355084
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  • 6. Genomic analysis of human chromosome 10q and 4q telomeres suggests a common origin.
    van Geel M, Dickson MC, Beck AF, Bolland DJ, Frants RR, van der Maarel SM, de Jong PJ, Hewitt JE.
    Genomics; 2002 Feb; 79(2):210-7. PubMed ID: 11829491
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  • 7. A large patient study confirming that facioscapulohumeral muscular dystrophy (FSHD) disease expression is almost exclusively associated with an FSHD locus located on a 4qA-defined 4qter subtelomere.
    Thomas NS, Wiseman K, Spurlock G, MacDonald M, Ustek D, Upadhyaya M.
    J Med Genet; 2007 Mar; 44(3):215-8. PubMed ID: 16987949
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  • 9. 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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  • 14. [Analysis of alleles 4qA and 4qB of the chromosome 4q subtelomere in Chinese Han population].
    Chen ZJ, Wang ZQ, Wu ZY, Wang N, Lin MT, Murong SX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun 02; 24(3):334-7. PubMed ID: 17557251
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  • 16. Facioscapulohumeral muscular dystrophy.
    Sacconi S, Salviati L, Desnuelle C.
    Biochim Biophys Acta; 2015 Apr 02; 1852(4):607-14. PubMed ID: 24882751
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