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Volumn 19, Issue SEPT., 2000, Pages 69-80

Facioscapulolimb muscular dystrophy (facioscapuloperoneal form of FSHD) in Russian families. Phenotype/genotype correlations

Author keywords

EcoRI; Facioscapulohumeral muscular dystrophy; Facioscapuloperoneal; Genetic heteroneity

Indexed keywords

DNA FRAGMENT;

EID: 0033787272     PISSN: 11282460     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (4)

References (25)
  • 3
    • 0002845499 scopus 로고
    • De la myopathie atrophique progressive (myopathie hereditaire debutant dans l'enfance par la face, sans alteration des systemes nerveux)
    • (1884) C.R. Acad. Sci. , vol.98 , pp. 53-55
    • Landouzy, L.1    Dejerine, J.2
  • 11
    • 0029433188 scopus 로고
    • History of the recognition and description of the facioscapulohumeral muscular dystrophy and on the priorities of Duchenne, Erb, Landouzy and Dejerine
    • (1995) Acta Cardiomiologica , vol.7 , pp. 79-84
    • Kazakov, V.M.1
  • 15
    • 4243459480 scopus 로고    scopus 로고
    • Some difficulties in defining the time when the first affection of mimic muscles appears in patients with autosomal dominat facioscapulolimb muscular dystrophy, type 2 (FSLD2) (or facioscapulohumeral)
    • (1997) Neuromusc. Disord. , vol.6-7 , pp. 443
    • Kazakov, V.M.1    Rudenko, D.I.2
  • 16
    • 0032468601 scopus 로고    scopus 로고
    • On the name of FSHD and the famous discussion between Erb and Landouzy-Dejerine once again. Part 1
    • (1998) Acta Myologica , vol.2 , pp. 72-74
    • Kazakov, V.M.1
  • 17
    • 0007687739 scopus 로고    scopus 로고
    • On the name of FSHD and the famous discussion between Erb and Landouzy-Dejerine once again. Part 2
    • (1999) Acta Myologica , vol.3 , pp. 172-174
    • Kazakov, V.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.