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

作者信息

Rasore-Quartino A, Vignola G, Camera G

出版信息

Pathologica. 1985 Jul-Aug;77(1050):449-55.

PMID:3834376

Abstract

摘要

相似文献

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

Pathologica. 1985 Jul-Aug;77(1050):449-55.

Prenatal sonographic appearance of foramina parietalia permagna.

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引用本文的文献

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

Eur J Hum Genet. 2006 Feb;14(2):151-8. doi: 10.1038/sj.ejhg.5201526.

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

J Med Genet. 2000 Dec;37(12):916-20. doi: 10.1136/jmg.37.12.916.

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.

Am J Hum Genet. 1996 Apr;58(4):734-42.

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