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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

204 related items for PubMed ID: 23573583

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  • 3. [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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  • 4. [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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  • 5. 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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  • 7. An inherited 4q35-EcoRI-DNA-fragment of 35 kb in a family with a sporadic case of facioscapulohumeral muscular dystrophy (FSHD).
    Busse K, Köhler J, Stegmann K, Pongratz D, Koch MC, Schreiber H.
    Neuromuscul Disord; 2000 Mar; 10(3):178-81. PubMed ID: 10734264
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  • 9. [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; 20(3):232-4. PubMed ID: 12778451
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  • 13. Molecular genetics of facioscapulohumeral muscular dystrophy (FSHD).
    Fisher J, Upadhyaya M.
    Neuromuscul Disord; 1997 Jan; 7(1):55-62. PubMed ID: 9132141
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  • 18. D4F104S1 deletion in facioscapulohumeral muscular dystrophy: phenotype, size, and detection.
    Lemmers RJ, Osborn M, Haaf T, Rogers M, Frants RR, Padberg GW, Cooper DN, van der Maarel SM, Upadhyaya M.
    Neurology; 2003 Jul 22; 61(2):178-83. PubMed ID: 12874395
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