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Journal Abstract Search

185 related items for PubMed ID: 8781186

  • 21. [Genetic analysis of facioscapulohumeral muscular dystrophy (FSHD)].
    Goto K, Song MD, Lee JH, Arahata K.
    Rinsho Shinkeigaku; 1995 Dec; 35(12):1416-8. PubMed ID: 8752415
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  • 23. Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35.
    van Deutekom JC, Lemmers RJ, Grewal PK, van Geel M, Romberg S, Dauwerse HG, Wright TJ, Padberg GW, Hofker MH, Hewitt JE, Frants RR.
    Hum Mol Genet; 1996 May; 5(5):581-90. PubMed ID: 8733123
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  • 24. Facioscapulohumeral muscular dystrophy. Phenotype-genotype correlation in patients with borderline D4Z4 repeat numbers.
    Butz M, Koch MC, Müller-Felber W, Lemmers RJ, van der Maarel SM, Schreiber H.
    J Neurol; 2003 Aug; 250(8):932-7. PubMed ID: 12928911
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  • 25. Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophy.
    van Overveld PG, Enthoven L, Ricci E, Rossi M, Felicetti L, Jeanpierre M, Winokur ST, Frants RR, Padberg GW, van der Maarel SM.
    Ann Neurol; 2005 Oct; 58(4):569-76. PubMed ID: 16178028
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  • 27. 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; 74(3):322-31. PubMed ID: 11708861
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  • 28. The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus.
    Wijmenga C, Winokur ST, Padberg GW, Skraastad MI, Altherr MR, Wasmuth JJ, Murray JC, Hofker MH, Frants RR.
    Hum Genet; 1993 Sep; 92(2):198-203. PubMed ID: 8103757
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  • 31. Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q.
    Jiang G, Yang F, van Overveld PG, Vedanarayanan V, van der Maarel S, Ehrlich M.
    Hum Mol Genet; 2003 Nov 15; 12(22):2909-21. PubMed ID: 14506132
    [Abstract] [Full Text] [Related]

  • 32. Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35.
    van Deutekom JC, Hofker MH, Romberg S, van Geel M, Rommens J, Wright TJ, Hewitt JE, Padberg GW, Wijmenga C, Frants RR.
    Muscle Nerve Suppl; 1995 Nov 15; (2):S19-26. PubMed ID: 23573582
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  • 33. Fine mapping of the FSHD gene region orientates the rearranged fragment detected by the probe p13E-11.
    Wright TJ, Wijmenga C, Clark LN, Frants RR, Williamson R, Hewitt JE.
    Hum Mol Genet; 1993 Oct 15; 2(10):1673-8. PubMed ID: 7903581
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  • 34. Chromatin loop domain organization within the 4q35 locus in facioscapulohumeral dystrophy patients versus normal human myoblasts.
    Petrov A, Pirozhkova I, Carnac G, Laoudj D, Lipinski M, Vassetzky YS.
    Proc Natl Acad Sci U S A; 2006 May 02; 103(18):6982-7. PubMed ID: 16632607
    [Abstract] [Full Text] [Related]

  • 35. Recent amplification of the human FRG1 gene during primate evolution.
    Grewal PK, van Geel M, Frants RR, de Jong P, Hewitt JE.
    Gene; 1999 Feb 04; 227(1):79-88. PubMed ID: 9931447
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  • 38. Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qter.
    Wijmenga C, Sandkuijl LA, Moerer P, van der Boorn N, Bodrug SE, Ray PN, Brouwer OF, Murray JC, van Ommen GJ, Padberg GW.
    Am J Hum Genet; 1992 Aug 04; 51(2):411-5. PubMed ID: 1642239
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