Literature DB >> 13818676

Nonfamilial and nonhereditary craniofacial dysostosis: a variant of Crouzon's disease.

F H DUNN.   

Abstract

Entities:  

Keywords:  HYPERTELORISM/case reports

Mesh：

Year:  1960        PMID： 13818676

Source DB:  PubMed          Journal:  Am J Roentgenol Radium Ther Nucl Med        ISSN： 0002-9580


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  1 in total

1.  Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11.

Authors:  O Bartsch; W Wuyts; W Van Hul; J T Hecht; P Meinecke; D Hogue; W Werner; B Zabel; G K Hinkel; C M Powell; L G Shaffer; P J Willems
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025
  1 in total

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