Literature DB >> 6047019

A familial syndrome of mental retardation in association with multiple congenital anomalies resembling the syndrome of Smith-Lemli-Opitz.

H Kenis, T W Hustinx.   

Abstract

Entities:  

Mesh：

Year:  1967        PMID： 6047019

Source DB:  PubMed          Journal:  Maandschr Kindergeneeskd        ISSN： 0024-869X


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  4 in total

1.  Smith-Lemli-Opitz syndrome: review and report of two affected siblings.

Authors:  V P Johnson
Journal:  Z Kinderheilkd       Date:  1975

Review 2.  The Smith-Lemli-Opitz syndrome.

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

3.  Syndrome of retardation with urogenital and skeletal anomalies (Smith-Lemli-Opitz syndrome): clinical features and mode of inheritance.

Authors:  L Dallaire
Journal:  J Med Genet       Date:  1969-06       Impact factor: 6.318

4.  [The Smith-Lemli-Opitz-syndrome].

Authors:  H Schumacher
Journal:  Z Kinderheilkd       Date:  1969
  4 in total

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