Literature DB >> 862305

The Smith-Lemli-Opitz syndrome. Report of a consanguineous Arab infant with bilateral focal renal dysplasia.

K F Akl, G S Khudr, V M Der Kaloustian, S S Najjar.   

Abstract

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Year:  1977        PMID： 862305     DOI： 10.1177/000992287701600717

Source DB:  PubMed          Journal:  Clin Pediatr (Phila)        ISSN： 0009-9228            Impact factor:   1.168


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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.  The Smith-Lemli-Opitz syndrome. A detailed pathological study as a clue to a etiological heterogeneity.

Authors:  E D Cherstvoy; G I Lazjuk; T I Ostrovskaya; I A Shved; G I Kravtzova; I W Lurie; A I Gerasimovich
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1984

Review 3.  Lethal acrodysgenital dwarfism: a severe lethal condition resembling Smith-Lemli-Opitz syndrome.

Authors:  M L Merrer; M L Briard; S Girard; N Mulliez; C Moraine; M C Imbert
Journal:  J Med Genet       Date:  1988-02       Impact factor: 6.318
  3 in total

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