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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

148 related items for PubMed ID: 23573581

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  • 2. Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35.
    Wijmenga C, Dauwerse HG, Padberg GW, Meyer N, Murray JC, Mills K, van Ommen GB, Hofker MH, Frants RR.
    Muscle Nerve Suppl; 1995; 2():S14-8. PubMed ID: 7739620
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  • 8. Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35.
    van Deutekom JC, Hofker MH, Romberg S, van Geel M, Rommens J, Wright TJ, Hewitt JE, Padberg GW, Wijmenga C, Frants RR.
    Muscle Nerve Suppl; 1995; 2():S19-26. PubMed ID: 7739621
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  • 9. Physical mapping evidence for a duplicated region on chromosome 10qter showing high homology with the facioscapulohumeral muscular dystrophy locus on chromosome 4qter.
    Deidda G, Cacurri S, Grisanti P, Vigneti E, Piazzo N, Felicetti L.
    Eur J Hum Genet; 1995; 3(3):155-67. PubMed ID: 7583041
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  • 11. 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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  • 12. Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD).
    Mills KA, Buetow KH, Xu Y, Ritty TM, Mathews KD, Bodrug SE, Wijmenga C, Balazs I, Murray JC.
    Am J Hum Genet; 1992 Aug 19; 51(2):432-9. PubMed ID: 1642243
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  • 13. Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qter.
    Wijmenga C, Sandkuijl LA, Moerer P, van der Boorn N, Bodrug SE, Ray PN, Brouwer OF, Murray JC, van Ommen GJ, Padberg GW.
    Am J Hum Genet; 1992 Aug 19; 51(2):411-5. PubMed ID: 1642239
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  • 17. Fine mapping of the FSHD gene region orientates the rearranged fragment detected by the probe p13E-11.
    Wright TJ, Wijmenga C, Clark LN, Frants RR, Williamson R, Hewitt JE.
    Hum Mol Genet; 1993 Oct 19; 2(10):1673-8. PubMed ID: 7903581
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  • 18. 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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  • 19. Application of chromosome 4q35-qter marker (pFR-1) for DNA rearrangement of facioscapulohumeral muscular dystrophy patients in Taiwan.
    Hsu YD, Kao MC, Shyu WC, Lin JC, Huang NE, Sun HF, Yang KD, Tsao WL.
    J Neurol Sci; 1997 Jul 19; 149(1):73-9. PubMed ID: 9168169
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  • 20. Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35.
    Mathews KD, Mills KA, Bosch EP, Ionasescu VV, Wiles KR, Buetow KH, Murray JC.
    Am J Hum Genet; 1992 Aug 19; 51(2):428-31. PubMed ID: 1642242
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