Literature DB >> 9714003

Syndromic foramina parietalia permagna.

K Chrzanowska1, K Kozlowski, A Kowalska.   

Abstract

We report on a boy with unique somatic and skeletal manifestations. The syndrome consists of branchial and auricular fistulae, abnormal face, and skeletal abnormalities including foramina parietalia permagna.

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Year:  1998        PMID： 9714003     DOI： 10.1002/(sici)1096-8628(19980806)78:5<401::aid-ajmg1>3.0.co;2-o

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


  2 in total

1.  Malformation of cortical and vascular development in one family with parietal foramina determined by an ALX4 homeobox gene mutation.

Authors:  Marcelo Valente; Kette D Valente; Sofia S M Sugayama; Chong Ae Kim
Journal:  AJNR Am J Neuroradiol       Date:  2004 Nov-Dec       Impact factor: 3.825

2.  Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype.

Authors:  Lampros A Mavrogiannis; Indira B Taylor; Sally J Davies; Feliciano J Ramos; José L Olivares; Andrew O M Wilkie
Journal:  Eur J Hum Genet       Date:  2006-02       Impact factor: 4.246
  2 in total

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