Literature DB >> 8911909

Diagnostic problems in congenital myotonic dystrophy.

M DiRocco, M Gennarelli, E Veneselli, M Bado, M Romanengo, M E Celle, G Cordone, C Borrone.   

Abstract

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Year:  1996        PMID： 8911909     DOI： 10.1007/bf02282900

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN： 0340-6199            Impact factor:   3.183


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  2 in total

1.  Instability versus predictability: the molecular diagnosis of myotonic dystrophy.

Authors:  G K Suthers; S M Huson; K E Davies
Journal:  J Med Genet       Date:  1992-11       Impact factor: 6.318

2.  Skeletal muscle in children with congenital myotonic dystrophy in the first year of life.

Authors:  W Müller-Felber; M Schmidt-Achert; D E Pongratz
Journal:  Clin Neuropathol       Date:  1993 Jul-Aug       Impact factor: 1.368
  2 in total
  1 in total

1.  CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy.

Authors:  Lise Barbé; Stella Lanni; Arturo López-Castel; Silvie Franck; Claudia Spits; Kathelijn Keymolen; Sara Seneca; Stephanie Tomé; Ioana Miron; Julie Letourneau; Minggao Liang; Sanaa Choufani; Rosanna Weksberg; Michael D Wilson; Zdenek Sedlacek; Cynthia Gagnon; Zuzana Musova; David Chitayat; Patrick Shannon; Jean Mathieu; Karen Sermon; Christopher E Pearson
Journal:  Am J Hum Genet       Date:  2017-03-02       Impact factor: 11.025
  1 in total

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