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

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

Heterozygous mutations of the homeobox genes ALX4 and MSX2 cause skull defects termed enlarged parietal foramina (PFM) and cranium bifidum (CB); a single MSX2 mutation has been documented in a unique craniosynostosis (CRS) family. However, the relative mutational contribution of these genes to PFM/C...

Bibliografiset tiedot
Päätekijät:	Mavrogiannis, L, Taylor, I, Davies, S, Ramos, F, Olivares, J, Wilkie, A
Aineistotyyppi:	Journal article
Kieli:	English
Julkaistu:	2006

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