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PUBMED FOR HANDHELDS

Journal Abstract Search

264 related items for PubMed ID: 8752415

  • 1. [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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  • 2. Cloning and mapping of a very short (10-kb) EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD).
    Lee JH, Goto K, Sahashi K, Nonaka I, Matsuda C, Arahata K.
    Muscle Nerve Suppl; 1995 Dec; 2():S27-31. PubMed ID: 7739622
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  • 3. [Facioscapulohumeral muscular dystrophy (FSHD)].
    Funakoshi M, Goto K, Kim BY, Arahata K.
    Nihon Rinsho; 1997 Dec; 55(12):3181-5. PubMed ID: 9436432
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  • 6. Characterization of a tandemly repeated 3.3-kb KpnI unit in the facioscapulohumeral muscular dystrophy (FSHD) gene region on chromosome 4q35.
    Lee JH, Goto K, Matsuda C, Arahata K.
    Muscle Nerve Suppl; 1995 Dec; 2():S6-13. PubMed ID: 7739628
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  • 9. FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit.
    van Deutekom JC, Wijmenga C, van Tienhoven EA, Gruter AM, Hewitt JE, Padberg GW, van Ommen GJ, Hofker MH, Frants RR.
    Hum Mol Genet; 1993 Dec; 2(12):2037-42. PubMed ID: 8111371
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  • 10. Two cases of chromosome 4q35-linked early onset facioscapulohumeral muscular dystrophy with mental retardation and epilepsy.
    Miura K, Kumagai T, Matsumoto A, Iriyama E, Watanabe K, Goto K, Arahata K.
    Neuropediatrics; 1998 Oct; 29(5):239-41. PubMed ID: 9810558
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  • 11. FSHD-like patients without 4q35 deletion.
    Yamanaka G, Goto K, Ishihara T, Oya Y, Miyajima T, Hoshika A, Nishino I, Hayashi YK.
    J Neurol Sci; 2004 Apr 15; 219(1-2):89-93. PubMed ID: 15050443
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  • 16. Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4.
    Deak KL, Lemmers RJ, Stajich JM, Klooster R, Tawil R, Frants RR, Speer MC, van der Maarel SM, Gilbert JR.
    Neurology; 2007 Feb 20; 68(8):578-82. PubMed ID: 17229919
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