Literature DB >> 3834376

Hereditary enlarged parietal foramina (foramina parietalia permagna). Prenatal diagnosis, evolution and family study.

A Rasore-Quartino, G Vignola, G Camera.   

Abstract

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Year:  1985        PMID： 3834376

Source DB:  PubMed          Journal:  Pathologica        ISSN： 0031-2983


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  3 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

2.  The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500).

Authors:  W Wuyts; E Cleiren; T Homfray; A Rasore-Quartino; F Vanhoenacker; W Van Hul
Journal:  J Med Genet       Date:  2000-12       Impact factor: 6.318

3.  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
  3 in total

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