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OtherPediatric Neuroimaging

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
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Kette D. Valente
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Sofia S. M. Sugayama
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Chong Ae Kim
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References

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    Little BB, Knoll KA, et al. Hereditary cranium bifidum and symmetric parietal foramina are the same entity. Am J Med Genet 1990;35:453–458
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    Chrzanowska K, Kozlowski K, Kowalska A. Syndromic foramina parietalia permagna. Am J Med Genet 1998;78:401–405
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    Wilkie AO, Tang Z, Elanko N, et al. Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification. Nat Genet 2000;24:387–390
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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
    Abstract/FREE Full Text
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    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
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    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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    Reddy AT, Hedlund GL, Percy AK. Enlarged parietal foramina:association with cerebral venous and cortical anomalies. Neurology 2000;54:1175–1178
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    Sener RN. Association of persistent falcine sinus with different clinicoradiologic conditions: MR imaging and MR angiography. Comput Med Imaging Graph 2000;24:343–348
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    Jones B, Ball WS, Tomsick TA, et al. Vein of Galen aneurysmal malformation: diagnosis and treatment of 13 children with extended clinical follow-up. AJNR Am J Neuroradiol 2002;23:1717–1724
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    Antonopoulou IM, Wilkie AOM, Morris-Kay GM. Functions of ALX4 and MSX2 in ossification of the skull vault. J Anatomy 2002;201:428–429
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    Rakic P, Sidman RL. Histogenesis of cortical layers in human cerebellum, particularly the lamina dissecans. J Comp Neurol 1970;139:473–500
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American Journal of Neuroradiology: 25 (10)
American Journal of Neuroradiology
Vol. 25, Issue 10
1 Nov 2004
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Cite this article
Marcelo Valente, Kette D. Valente, Sofia S. M. Sugayama, Chong Ae Kim
Malformation of Cortical and Vascular Development in One Family with Parietal Foramina Determined by an ALX4 Homeobox Gene Mutation
American Journal of Neuroradiology Nov 2004, 25 (10) 1836-1839;

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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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