1Glass HC, Shaw GM, Ma C, et al. Agenesis of the corpus callosum in California 1983-2003 : a population-based study. Am J Med Genet A, 2008,146A :2495-2500.
2Alvarez-DM, Cuadrado A, Navarro-Yubero C, et al. Regulation of the L1 cell adhesion molecule by thyroid hormone in the developing brain. Mol Cell Neurosci, 2000,16: 499-514.
3Evrard SG,Vega MD, Ramos AJ, et al. Altered neuron - glia interactions in a low, chronic prenatal ethanol exposure. Brain Res, 2003, 147 : 119-133.
4Bedeschi MF, Bonaglia MC, Grasso R, et al. Agenesis of the corpus callosum: clinical and genetic study in 63 young patients. Pediatr Neurol, 2006, 34: 186-193.
5Riverol M, Samaranch L, Pascual B. Forceps minor region signal abnormality " ears of the lynx" : an early MRI finding in spastic paraparesis with thin corpus callosum and mutations in the spatacsin gene (SPG11) on chromosome 15. J Neuroimaging, 2009,19:52-60.
6Alice AA, Nourhan AS, Dominika S, et al. Expanding the Clinical Spectrum of SPGll Gene Mutations in Recessive Hereditary Spastic Paraplegia with Thin Corpus Callosum. Eur J Med Genet, 2011, 54: 82-85.
7Simpson MA, CrossH, ProukakisC, et al. Maspardin is mutated in mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementia. Am J Hum Genet, 2003,73 : 1147-1156.
8Alkan A, Kutlu R, Baysal T, et al. Associated brain anomalies and clinical findings in corpus callosum dysgenesis. Tani Girisim Radyol,2003 ,9 :411-417.
9Hetts SW, Sherr EH, Chao S, et al. Anomalies of the corpuscallosum: an MR analysis of the phenotypic spectrum of associated malformations. AIR Am J Roentgenol, 2006, 187: 1343-1348.