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Journal Abstract Search

144 related items for PubMed ID: 9680377

  • 1. 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
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  • 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 Aug; (2):S98-102. PubMed ID: 23573594
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  • 4. 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
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  • 5. 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 Jun; 2():S98-102. PubMed ID: 7739634
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  • 6. 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
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  • 7. 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
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  • 10. 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
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  • 14. YAC contigs for 4q35 in the region of the facioscapulohumeral muscular dystrophy (FSHD) gene.
    Weiffenbach B, Dubois J, Manning S, Ma NS, Schutte BC, Winokur ST, Altherr MR, Jacobsen SJ, Stanton VP, Yokoyama K.
    Genomics; 1994 Feb 19; 19(3):532-41. PubMed ID: 8188296
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  • 15. 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 19; 5(5):581-90. PubMed ID: 8733123
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  • 18. Inter- and intrachromosomal sub-telomeric rearrangements on 4q35: implications for facioscapulohumeral muscular dystrophy (FSHD) aetiology and diagnosis.
    Lemmers RJ, van der Maarel SM, van Deutekom JC, van der Wielen MJ, Deidda G, Dauwerse HG, Hewitt J, Hofker M, Bakker E, Padberg GW, Frants RR.
    Hum Mol Genet; 1998 Aug 19; 7(8):1207-14. PubMed ID: 9668160
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  • 20. High resolution fluorescence in situ hybridization to linearly extended DNA visually maps a tandem repeat associated with facioscapulohumeral muscular dystrophy immediately adjacent to the telomere of 4q.
    Bengtsson U, Altherr MR, Wasmuth JJ, Winokur ST.
    Hum Mol Genet; 1994 Oct 19; 3(10):1801-5. PubMed ID: 7849703
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