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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

193 related items for PubMed ID: 7739624

  • 1. The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qter.
    Bakker E, Wijmenga C, Vossen RH, Padberg GW, Hewitt J, van der Wielen M, Rasmussen K, Frants RR.
    Muscle Nerve Suppl; 1995; 2():S39-44. PubMed ID: 7739624
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  • 2. The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qter.
    Bakker E, Wijmenga C, Vossen RH, Padberg GW, Hewitt J, van der Wielen M, Rasmussen K, Frants RR.
    Muscle Nerve Suppl; 1995; (2):S39-44. PubMed ID: 23573585
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  • 10. 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; 36(11):823-8. PubMed ID: 10544225
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  • 15. Cloning and mapping of a very short (10-kb) EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD).
    Lee JH, Goto K, Sahashi KO, Nonaka I, Matsuda C, Arahata K.
    Muscle Nerve Suppl; 1995 Nov; (2):S27-31. PubMed ID: 23573583
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  • 16. [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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  • 20. Definitive molecular diagnosis of facioscapulohumeral dystrophy.
    Orrell RW, Tawil R, Forrester J, Kissel JT, Mendell JR, Figlewicz DA.
    Neurology; 1999 Jun 10; 52(9):1822-6. PubMed ID: 10371529
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