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Journal Abstract Search

144 related items for PubMed ID: 9680377

  • 21. A molecular genetic linkage map of mouse chromosome 7.
    Saunders AM, Seldin MF.
    Genomics; 1990 Nov; 8(3):525-35. PubMed ID: 1981054
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  • 22. A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD).
    Winokur ST, Schutte B, Weiffenbach B, Washington SS, McElligott D, Chakravarti A, Wasmuth JH, Altherr MR.
    Am J Hum Genet; 1993 Oct; 53(4):874-80. PubMed ID: 8213815
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  • 25. YAC contigs of the Rab1 and wobbler (wr) spinal muscular atrophy gene region on proximal mouse chromosome 11 and of the homologous region on human chromosome 2p.
    Wedemeyer N, Lengeling A, Ronsiek M, Korthaus D, Baer K, Wuttke M, Jockusch H.
    Genomics; 1996 Mar 15; 32(3):447-54. PubMed ID: 8838809
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  • 27. Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD).
    Cacurri S, Deidda G, Piazzo N, Novelletto A, La Cesa I, Servidei S, Galluzzi G, Wijmenga C, Frants RR, Felicetti L.
    Hum Genet; 1994 Oct 15; 94(4):367-74. PubMed ID: 7927331
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  • 29. Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization.
    Wijmenga C, Padberg GW, Moerer P, Wiegant J, Liem L, Brouwer OF, Milner EC, Weber JL, van Ommen GB, Sandkuyl LA.
    Genomics; 1991 Apr 15; 9(4):570-5. PubMed ID: 2037288
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  • 30. 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 15; 149(1):73-9. PubMed ID: 9168169
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  • 32. Physical mapping and YAC-cloning connects four genetically distinct 4qter loci (D4S163, D4S139, D4F35S1 and D4F104S1) in the FSHD gene-region.
    Wijmenga C, Wright TJ, Baan MJ, Padberg GW, Williamson R, van Ommen GJ, Hewitt JE, Hofker MH, Frants RR.
    Hum Mol Genet; 1993 Oct 15; 2(10):1667-72. PubMed ID: 8268920
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  • 33. Comparative mapping of distal murine chromosome 11 and human 17q21.3 in a region containing a modifying locus for murine plasma von Willebrand factor level.
    Mohlke KL, Purkayastha AA, Westrick RJ, Ginsburg D.
    Genomics; 1998 Nov 15; 54(1):19-30. PubMed ID: 9806826
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  • 34. 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 Nov 15; (2):S19-26. PubMed ID: 23573582
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  • 35. Integrated radiation hybrid map of human chromosome 2p13: possible involvement of dynactin in neuromuscular diseases.
    Korthaus D, Wedemeyer N, Lengeling A, Ronsiek M, Jockusch H, Schmitt-John T.
    Genomics; 1997 Jul 15; 43(2):242-4. PubMed ID: 9244444
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  • 38. Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromsome 4q35 recombination events.
    Weiffenbach B, Dubois J, Storvick D, Tawil R, Jacobsen SJ, Gilbert J, Wijmenga C, Mendell JR, Winokur S, Altherr MR.
    Nat Genet; 1993 Jun 15; 4(2):165-9. PubMed ID: 8102297
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  • 39. The mapping of a cDNA from the human X-linked Duchenne muscular dystrophy gene to the mouse X chromosome.
    Brockdorff N, Cross GS, Cavanna JS, Fisher EM, Lyon MF, Davies KE, Brown SD.
    Nature; 1993 Jun 15; 328(6126):166-8. PubMed ID: 3600793
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  • 40. A linkage map of mouse chromosome 19: definition of comparative mapping relationships with human chromosomes 10 and 11 including the MEN1 locus.
    Rochelle JM, Watson ML, Oakey RJ, Seldin MF.
    Genomics; 1992 Sep 15; 14(1):26-31. PubMed ID: 1358795
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