Literature DB >> 7776805

Prenatal diagnosis in congenital muscular dystrophy.

F Muntoni, C Sewry, L Wilson, C Angelini, C P Trevisan, B Brambati, V Dubowitz.   

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Year:  1995        PMID： 7776805     DOI： 10.1016/s0140-6736(95)90504-9

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  3 in total

1.  Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophy.

Authors:  I S Naom; M D'Alessandro; H Topaloglu; C Sewry; A Ferlini; A Helbling-Leclerc; P Guicheney; J Weissenbach; K Schwartz; K Bushby; J Philpot; V Dubowitz; F Muntoni
Journal:  J Med Genet       Date:  1997-02       Impact factor: 6.318

2.  Congenital muscular dystrophy with laminin alpha 2 chain deficiency: identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry.

Authors:  R Herrmann; V Straub; K Meyer; T Kahn; M Wagner; T Voit
Journal:  Eur J Pediatr       Date:  1996-11       Impact factor: 3.183

3.  Expression of laminin subunits in human fetal skeletal muscle.

Authors:  C A Sewry; M Chevallay; F M Tomé
Journal:  Histochem J       Date:  1995-07
  3 in total

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