OtherPEDIATRICS
Malformation of Cortical and Vascular Development in One Family with Parietal Foramina Determined by an ALX4 Homeobox Gene Mutation
Marcelo Valente, Kette D. Valente, Sofia S. M. Sugayama and Chong Ae Kim
American Journal of Neuroradiology November 2004, 25 (10) 1836-1839;
Marcelo Valente
Kette D. Valente
Sofia S. M. Sugayama
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- ↵Wuyts W, Cleiren E, Homfray T, et al. The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500). J Med Genet 2000;37:916–920
- ↵Wu YQ, Badano JL, McCaskill C, et al. Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome. Am J Hum Genet 2000;67:1327–1332
- ↵Mavrogiannis LA, Antonopoulou I, Baxova A, et al. Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects. Nat Genet 2001;27:17–18
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Malformation of Cortical and Vascular Development in One Family with Parietal Foramina Determined by an ALX4 Homeobox Gene Mutation
Marcelo Valente, Kette D. Valente, Sofia S. M. Sugayama, Chong Ae Kim
American Journal of Neuroradiology Nov 2004, 25 (10) 1836-1839;
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