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Volumn 7, Issue 3, 1997, Pages 176-179

Prenatal diagnosis in merosin-deficient congenital muscular dystrophy

Author keywords

Merosin deficient; Muscular dystrophy; Prenatal

Indexed keywords

LAMININ; MEROSIN;

EID: 0030943859     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-8966(97)00448-3     Document Type: Article
Times cited : (21)

References (10)
  • 2
    • 0028094441 scopus 로고
    • Localisation of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping
    • Hillaire D, Leclerc A, Faure S et al. Localisation of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping. Hum Mol Genet 1994;3:1657-61.
    • (1994) Hum Mol Genet , vol.3 , pp. 1657-1661
    • Hillaire, D.1    Leclerc, A.2    Faure, S.3
  • 7
    • 0028584463 scopus 로고
    • Prenatal detection of merosin expression in human placenta
    • Voit T; Fardeau M, Tome FM. Prenatal detection of merosin expression in human placenta. Neuropediatrics 1994:25:332-333.
    • (1994) Neuropediatrics , vol.25 , pp. 332-333
    • Voit, T.1    Fardeau, M.2    Tome, F.M.3
  • 10
    • 0342914573 scopus 로고
    • Genetic mapping with microsatellites
    • Richwood D, Hames BD, editors London: Oxford University Press
    • Naom IS, Mathew CG, Town M. Genetic mapping with microsatellites. In: Richwood D, Hames BD, editors. DNA cloning: complex genomes, second edition. London: Oxford University Press, 1995:195-217.
    • (1995) DNA Cloning: Complex Genomes, Second Edition , pp. 195-217
    • Naom, I.S.1    Mathew, C.G.2    Town, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.