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Journal Abstract Search

107 related items for PubMed ID: 7602333

  • 1. Phenotypic and pathologic evaluation of the myd mouse. A candidate model for facioscapulohumeral dystrophy.
    Mathews KD, Rapisarda D, Bailey HL, Murray JC, Schelper RL, Smith R.
    J Neuropathol Exp Neurol; 1995 Jul; 54(4):601-6. PubMed ID: 7602333
    [Abstract] [Full Text] [Related]

  • 2. Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q.
    Mathews KD, Mills KA, Bailey HL, Schelper RL, Murray JC.
    Muscle Nerve Suppl; 1995 Jul; 2():S98-102. PubMed ID: 7739634
    [Abstract] [Full Text] [Related]

  • 3. Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q.
    Mathews KD, Mills KA, Bailey HL, Schelper RL, Murray JC.
    Muscle Nerve Suppl; 1995 Jul; (2):S98-102. PubMed ID: 23573594
    [Abstract] [Full Text] [Related]

  • 4. The molecular genetics of human facioscapulohumeral muscular dystrophy and the myodystrophy mouse model.
    Mathews KD, Mills KA.
    Curr Opin Neurol; 1996 Oct; 9(5):394-9. PubMed ID: 8894417
    [Abstract] [Full Text] [Related]

  • 5. Genetic mapping near the myd locus on mouse chromosome 8.
    Mills KA, Mathews KD, Scherpbier-Heddema T, Schelper RL, Schmalzel R, Bailey HL, Nadeau JH, Buetow KH, Murray JC.
    Mamm Genome; 1995 Apr; 6(4):278-80. PubMed ID: 7613034
    [Abstract] [Full Text] [Related]

  • 6. The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8.
    Grewal PK, van Deutekom JC, Mills KA, Lemmers RJ, Mathews KD, Frants RR, Hewitt JE.
    Mamm Genome; 1997 Jun; 8(6):394-8. PubMed ID: 9166581
    [Abstract] [Full Text] [Related]

  • 7. High-resolution mapping of mouse chromosome 8 identifies an evolutionary chromosomal breakpoint.
    Grewal PK, Bolland DJ, Todd LC, Hewitt JE.
    Mamm Genome; 1998 Aug; 9(8):603-7. PubMed ID: 9680377
    [Abstract] [Full Text] [Related]

  • 8. Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletions.
    Trevisan CP, Pastorello E, Tomelleri G, Vercelli L, Bruno C, Scapolan S, Siciliano G, Comacchio F.
    Eur J Neurol; 2008 Dec; 15(12):1353-8. PubMed ID: 19049553
    [Abstract] [Full Text] [Related]

  • 9. Sensorineural hearing loss in the mdx mouse: a model of Duchenne muscular dystrophy.
    Raynor EM, Mulroy MJ.
    Laryngoscope; 1997 Aug; 107(8):1053-6. PubMed ID: 9261007
    [Abstract] [Full Text] [Related]

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  • 11. Mutant glycosyltransferase and altered glycosylation of alpha-dystroglycan in the myodystrophy mouse.
    Grewal PK, Holzfeind PJ, Bittner RE, Hewitt JE.
    Nat Genet; 2001 Jun; 28(2):151-4. PubMed ID: 11381262
    [Abstract] [Full Text] [Related]

  • 12. [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
    [Abstract] [Full Text] [Related]

  • 13. Facioscapulohumeral muscular dystrophy and accompanying hearing loss.
    Meyerson MD, Lewis E, Ill K.
    Arch Otolaryngol; 1984 Apr; 110(4):261-6. PubMed ID: 6704043
    [Abstract] [Full Text] [Related]

  • 14. Facioscapulohumeral dystrophy with cochlear hearing loss and tortuosity of retinal vessels.
    Gieron MA, Korthals JK, Kousseff BG.
    Am J Med Genet; 1985 Sep; 22(1):143-7. PubMed ID: 4050849
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  • 15. The auditory, vestibular, and oculomotor system in facioscapulohumeral dystrophy.
    Verhagen WI, Huygen PL, Padberg GW.
    Acta Otolaryngol Suppl; 1995 Sep; 520 Pt 1():140-2. PubMed ID: 8749103
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  • 17. Facioscapulohumeral muscular dystrophy: clinical diversity and genetic abnormalities in Japanese patients.
    Nakagawa M, Matsuzaki T, Higuchi I, Fukunaga H, Inui T, Nagamitsu S, Yamada H, Arimura K, Osame M.
    Intern Med; 1997 May; 36(5):333-9. PubMed ID: 9213170
    [Abstract] [Full Text] [Related]

  • 18. Towards the finer mapping of facioscapulohumeral muscular dystrophy at 4q35: construction of a laser microdissection library.
    Upadhyaya M, Osborn M, Maynard J, Altherr M, Ikeda J, Harper PS.
    Am J Med Genet; 1995 Jun 19; 60(3):244-51. PubMed ID: 7573180
    [Abstract] [Full Text] [Related]

  • 19. [Progress in researches on the molecular genetics of facioscapulohumeral muscular dystrophy].
    Su Q, Zhang C.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Oct 19; 18(5):398-401. PubMed ID: 11592052
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