Literature DB >> 7670261

Aplasia cutis congenita and enlarged parietal foramina (Catlin marks) in a family.

S Preis1, V Engelbrecht, H G Lenard.   

Abstract

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Mesh：

Year:  1995        PMID： 7670261     DOI： 10.1111/j.1651-2227.1995.tb13735.x

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN： 0803-5253            Impact factor:   2.299


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  3 in total

1.  A novel mutation in the MSX2 homeobox gene of a family with foramina parietalia permagna, headache and vascular anomaly.

Authors:  Michella Ghassibé; Vincent Bernier; Laurence M Boon; Miikka Vikkula
Journal:  Eur J Pediatr       Date:  2006-04-27       Impact factor: 3.183

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

Review 3.  Enlarged parietal foramina: a review of genetics, prognosis, radiology, and treatment.

Authors:  Christoph J Griessenauer; Philip Veith; Martin M Mortazavi; Carrie Stewart; Angela Grochowsky; Marios Loukas; R Shane Tubbs
Journal:  Childs Nerv Syst       Date:  2012-12-04       Impact factor: 1.475
  3 in total

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