Literature DB >> 13605357

Congenital micrognathia.

C M WESEMAN.   

Abstract

Entities:  

Keywords:  MANDIBLE/abnormalities

Mesh：

Year:  1959        PMID： 13605357     DOI： 10.1001/archotol.1959.00730030035005

Source DB:  PubMed          Journal:  AMA Arch Otolaryngol        ISSN： 0096-6894


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  3 in total

1.  Pierre Robin syndrome: autosomal dominant inheritance with pleiotropic effect.

Authors:  S S Sidhu; R N Deshmukh
Journal:  Indian J Pediatr       Date:  1989 May-Jun       Impact factor: 1.967

2.  [Profile changes in patients with Pierre Robin syndrome].

Authors:  S Zschiesche
Journal:  Fortschr Kieferorthop       Date:  1984-04

3.  The Robin anomalad (Pierre Robin syndrome)--a follow up study.

Authors:  A J Williams; M A Williams; C A Walker; P G Bush
Journal:  Arch Dis Child       Date:  1981-09       Impact factor: 3.791
  3 in total

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