Literature DB >> 7778591

Prenatal diagnosis of Smith-Lemli-Opitz syndrome.

F J Stewart, N C Nevin, J C Dornan.   

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Year:  1995        PMID： 7778591     DOI： 10.1002/ajmg.1320560310

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  3 in total

Review 1.  The Smith-Lemli-Opitz syndrome.

Authors:  R I Kelley; R C Hennekam
Journal:  J Med Genet       Date:  2000-05       Impact factor: 6.318

2.  Smith-Lemli-Opitz syndrome: a variable clinical and biochemical phenotype.

Authors:  A K Ryan; K Bartlett; P Clayton; S Eaton; L Mills; D Donnai; R M Winter; J Burn
Journal:  J Med Genet       Date:  1998-07       Impact factor: 6.318

3.  Smith-Lemli-Opitz syndrome - Fetal phenotypes with special reference to the syndrome-specific internal malformation pattern.

Authors:  Katharina Schoner; Martina Witsch-Baumgartner; Jana Behunova; Robert Petrovic; Rainer Bald; Susanne G Kircher; Annette Ramaswamy; Britta Kluge; Matthias Meyer-Wittkopf; Ralf Schmitz; Barbara Fritz; Johannes Zschocke; Franco Laccone; Helga Rehder
Journal:  Birth Defects Res       Date:  2019-12-16       Impact factor: 2.344
  3 in total

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