Spectrum of corpus callosum agenesisSZTRIHA, Laszlo.Pediatric neurology. 2005, Vol 32, Num 2, pp 94-101, issn 0887-8994, 8 p.Article

Partial Agenesis of Corpus Callosum in Sanjad-Sakati Syndrome (p-ACC)ALGHASAB, Naif; JANATI, A. Bruce; KHAN, Aslam et al.Canadian journal of neurological sciences. 2012, Vol 39, Num 6, pp 833-834, issn 0317-1671, 2 p.Article

Chromosome lq42 deletion and agenesis of the corpus callosumPUTHURAN, Mani J; ROWLAND-HILL, Christopher A; SIMPSON, J et al.American journal of medical genetics. 2005, Vol 138A, Num 1, pp 68-69, issn 0148-7299, 2 p.Article

Clinical and molecular characteristics of 1qter microdeletion syndrome : delineating a critical region for corpus callosum agenesis/hypogenesisVAN BON, B. W. M; KOOLEN, D. A; NOVARA, F et al.Journal of medical genetics. 2008, Vol 45, Num 6, pp 346-354, issn 0022-2593, 9 p.Article

Agenesis of the corpus callosum : Lessons from humans and miceKAMNASARAN, Deepak.Clinical and investigative medicine. 2005, Vol 28, Num 5, pp 267-282, issn 0147-958X, 16 p.Article

Comprehension of humor in primary agenesis of the corpus callosumBROWN, Warren S; PAUL, Lynn K; SYMINGTON, Melissa et al.Neuropsychologia. 2005, Vol 43, Num 6, pp 906-916, issn 0028-3932, 11 p.Article

Corpus Callosum Agenesis in Trisomy 8pll.23 and Monosomy 4q34 Because of Maternal TranslocationISIK, Ugur; BASARAN, Seher; DEHGAN, Tahir et al.Pediatric neurology. 2008, Vol 39, Num 1, pp 55-57, issn 0887-8994, 3 p.Article

Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesisBAALA, Lekbir; BRIAULT, Sylvain; ATTIE-BITACH, Tania et al.Nature genetics. 2007, Vol 39, Num 4, pp 454-456, issn 1061-4036, 3 p.Article

Agenesis of the corpus callosum : Clinical and genetic study in 63 young patientsBEDESCHI, Maria Francesca; BONAGLIA, Maria Clara; BASSI, Maria Teresa et al.Pediatric neurology. 2006, Vol 34, Num 3, pp 186-193, issn 0887-8994, 8 p.Article

Neuroimaging in nine patients with inversion duplication of the short arm of chromosome 8FEENSTRA, I; VAN RAVENSWAAIJ, C. M. A; VAN DER KNAAP, M. S et al.Neuropediatrics. 2006, Vol 37, Num 2, pp 83-87, issn 0174-304X, 5 p.Article

Rare Combination of Gelastic Epilepsy, Agenesis of the Corpus Callosum, and HamartomaCHEN, Chia-Chun; LIN, Yu-Ting; CHANG, Wen-Cheng et al.Pediatric neurology. 2011, Vol 45, Num 4, pp 265-267, issn 0887-8994, 3 p.Article

Agénésie du corps calleux révélée par une encéphalocèle = Corpus callous agenesis revealed by an encephaloceleKAM, L; DAO, F; DIALLO, O et al.Journal de pédiatrie et de puériculture. 2007, Vol 20, Num 2, pp 74-77, issn 0987-7983, 4 p.Article

Dandy-Walker syndrome and corpus callosum agenesis in 5p deletionVIALARD, F; ROBYR, R; HILLION, Y et al.Prenatal diagnosis. 2005, Vol 25, Num 4, pp 311-313, issn 0197-3851, 3 p.Article

Novel movement disorder of the lower lip : Is it epilepsia partialis continua? Clues from a secondary caseWALI, Gurusidheshwar M.Movement disorders. 2005, Vol 20, Num 7, pp 903-904, issn 0885-3185, 2 p.Article

Agenesis of the corpus callosum and autism: a comprehensive comparisonPAUL, Lynn K; CORSELLO, Christina; KENNEDY, Daniel P et al.Brain. 2014, Vol 137, pp 1813-1829, issn 0006-8950, 17 p., 6Article

Exclusion of Mutations in TGIF, ALX3, and ALX4 Genes in Patients With the Syndrome of Frontonasal Dysgenesis, Callosal Agenesis, Basal Encephalocele, and Eye AnomaliesRIBEIRO-BICUDO, Lucilene Arilho; QUIEZI, Rodrigo G; GUION-ALMEIDA, Maria Leine et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 5, pp 1233-1235, issn 1552-4825, 3 p.Article

Genetic and Functional Analyses Identify DISC1 as a Novel Callosal Agenesis Candidate GeneOSBUN, Nathan; JIANG LI; PENNACCHIO, Len A et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 8, pp 1865-1876, issn 1552-4825, 12 p.Article

Congenital cervical teratoma, associated with agenesis of corpus callosum and a subarachnoid cystGOLDSTEIN, Israel; DRUGAN, Arie.Prenatal diagnosis. 2005, Vol 25, Num 6, pp 439-441, issn 0197-3851, 3 p.Article

Delineation of the cryptic 1qter deletion phenotypeMERRITT, J. Lawrence; YING ZOU; JALAL, Syed M et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 6, pp 599-603, issn 1552-4825, 5 p.Article

Patterned Neuropathologic Events Occurring in hyh Congenital Hydrocephalic Mutant MicePAEZ, Patricia; BATIZ, Luis-Federico; ROALES-BUJAN, Ruth et al.Journal of neuropathology and experimental neurology. 2007, Vol 66, Num 12, pp 1082-1092, issn 0022-3069, 11 p.Article

Neuroendoscopic management of interhemispheric cysts in childrenCINALLI, Giuseppe; PERETTA, Paola; MAGGI, Giuseppe et al.Journal of neurosurgery. Pediatrics. 2006, Vol 105, Num 3, pp 194-202, issn 1933-0707, 9 p.Article

Subtotal corpus callosum agenesis with recurrent hyperhidrosis-hypothermia (Shapiro syndrome)TAMBASCO, Nicola; COREA, Francesco; BOCOLA, Vittorio et al.Neurology. 2005, Vol 65, Num 1, issn 0028-3878, p. 124Article

Paralinguistic processing in children with callosal agenesis: Emergence of neurolinguistic deficitsBROWN, Warren S; SYMINGTION, Melissa; VANLANCKER-SIDTIS, Diana et al.Brain and language (Print). 2005, Vol 93, Num 2, pp 135-139, issn 0093-934X, 5 p.Article

Frontonasal Dysplasia, Callosal Agenesis, Basal Encephalocele, and Eye Anomalies Syndrome With a Partial 21q22.3 DeletionGUION-ALMEIDA, Maria Leine; RICHIERI-COSTA, Antonio; SARQUIS JEHEE, Fernanda et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 7, pp 1676-1679, issn 1552-4825, 4 p.Article

Prenatal MR Diffusion Tractography in a Fetus with Complete Corpus Callosum AgenesisMEODED, A; PORETTI, A; TEKES, A et al.Neuropediatrics. 2011, Vol 42, Num 3, pp 122-123, issn 0174-304X, 2 p.Article