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...
প্রধান লেখক: | Mavrogiannis, L, Taylor, I, Davies, S, Ramos, F, Olivares, J, Wilkie, A |
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বিন্যাস: | Journal article |
ভাষা: | English |
প্রকাশিত: |
2006
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অনুরূপ উপাদানগুলি
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Enlarged parietal foramina
অনুযায়ী: Mavrogiannis, L, অন্যান্য
প্রকাশিত: (2019) -
Parietal foramina with cleidocranial dysplasia is caused by mutation in MSX2.
অনুযায়ী: Garcia-Miñaur, S, অন্যান্য
প্রকাশিত: (2003) -
The roles of the homeobox genes ALX4 and MSX2 in skull development
অনুযায়ী: Mavrogiannis, L
প্রকাশিত: (2004) -
Alx4 and Msx2 play phenotypically similar and additive roles in skull vault differentiation.
অনুযায়ী: Antonopoulou, I, অন্যান্য
প্রকাশিত: (2004) -
Multiple Occipital, Parietal, Temporal, and Frontal Foramina: A Variant of Enlarged Parietal Foramina in an Infant
অনুযায়ী: Erdem Yılmaz, অন্যান্য
প্রকাশিত: (2014-12-01)