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Volumn 16, Issue 9-10, 2006, Pages 615-617

Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; CAUCASIAN; CHROMOSOME 4Q; COST; DIAGNOSTIC ACCURACY; DNA PROBE; EARLY DIAGNOSIS; FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; GENOTYPE; HUMAN; JAPAN; LETTER; LONG RANGE POLYMERASE CHAIN REACTION; NUCLEOTIDE REPEAT; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RAPID DIAGNOSIS; RESEARCH SUBJECT; SOUTHERN BLOTTING;

EID: 33748519219     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.nmd.2006.07.013     Document Type: Letter
Times cited : (13)

References (9)
  • 1
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    • Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy
    • Goto K., Nishino I., and Hayashi Y.K. Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy. Neuromuscul Disord 16 (2006) 256-261
    • (2006) Neuromuscul Disord , vol.16 , pp. 256-261
    • Goto, K.1    Nishino, I.2    Hayashi, Y.K.3
  • 2
    • 0026922062 scopus 로고
    • Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy
    • Wijmenga C., Hewitt J.E., Sandkuijl L.A., et al. Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy. Nat Genet 2 (1992) 26-30
    • (1992) Nat Genet , vol.2 , pp. 26-30
    • Wijmenga, C.1    Hewitt, J.E.2    Sandkuijl, L.A.3
  • 3
    • 0030052273 scopus 로고    scopus 로고
    • Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial cases
    • Bakker E., van der Wielen M.J., Voorhoeve E., et al. Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial cases. J Med Genet 33 (1996) 29-35
    • (1996) J Med Genet , vol.33 , pp. 29-35
    • Bakker, E.1    van der Wielen, M.J.2    Voorhoeve, E.3
  • 4
    • 0029017568 scopus 로고
    • DNA rearrangements in Japanese facioscapulohumeral muscular dystrophy patients: clinical correlations
    • Goto K., Lee J.H., Matsuda C., et al. DNA rearrangements in Japanese facioscapulohumeral muscular dystrophy patients: clinical correlations. Neuromuscul Disord 5 (1995) 201-208
    • (1995) Neuromuscul Disord , vol.5 , pp. 201-208
    • Goto, K.1    Lee, J.H.2    Matsuda, C.3
  • 5
    • 0030949864 scopus 로고    scopus 로고
    • Application of chromosome 4q35-qter marker (pFR-1) for DNA rearrangement of facioscapulohumeral muscular dystrophy patients in Taiwan
    • Hsu Y.D., Kao M.C., Shyu W.C., et al. Application of chromosome 4q35-qter marker (pFR-1) for DNA rearrangement of facioscapulohumeral muscular dystrophy patients in Taiwan. J Neurol Sci 149 (1997) 73-79
    • (1997) J Neurol Sci , vol.149 , pp. 73-79
    • Hsu, Y.D.1    Kao, M.C.2    Shyu, W.C.3
  • 8
  • 9
    • 0029038951 scopus 로고
    • Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD)
    • Lunt P.W., Jardine P.E., Koch M.C., et al. Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD). Hum Mol Genet 4 (1995) 951-958
    • (1995) Hum Mol Genet , vol.4 , pp. 951-958
    • Lunt, P.W.1    Jardine, P.E.2    Koch, M.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.