Classification of the cerebro-oculo-muscular syndrome(s). Commentary to Kimura's paper (pp. 182-91)DOBYNS, W. B.Brain & development (Tokyo. 1979). 1993, Vol 15, Num 3, pp 242-244, issn 0387-7604Article

Agenesis of the corpus callosum and gyral malformations are frequent manifestations of nonketotic hyperglycinemiaDOBYNS, W. B.Neurology. 1989, Vol 39, Num 6, pp 817-820, issn 0028-3878Article

Absence makes the search grow longerDOBYNS, W. B.American journal of human genetics. 1996, Vol 58, Num 1, pp 7-16, issn 0002-9297Article

Bilateral periventricular nodular heterotopia with mental retardation and frontonasal malformationGUERRINI, R; DOBYNS, W. B.Neurology. 1998, Vol 51, Num 2, pp 499-503, issn 0028-3878Article

Agenesis of the corpus callosum and Dandy-Walker malformation associated with hemimegalencephaly in the sebaceous nevus syndromeDODGE, N. N; DOBYNS, W. B.American journal of medical genetics. 1995, Vol 56, Num 2, pp 147-150, issn 0148-7299Article

Lissencephaly with cerebellar hypoplasia (LCH): A heterogeneous group of cortical malformationsROSS, M. E; SWANSON, K; DOBYNS, W. B et al.Neuropediatrics. 2001, Vol 32, Num 5, pp 256-263, issn 0174-304XArticle

Lissencephaly and other malformations of cortical development : 1995 updateDOBYNS, W. B; TRUWIT, C. L.Neuropediatrics. 1995, Vol 26, Num 3, pp 132-147, issn 0174-304XArticle

Vascular abnormalities in epidermal nevus syndromeDOBYNS, W. B; GARG, B. P.Neurology. 1991, Vol 41, Num 2, pp 276-278, issn 0028-3878, 3 p., p.1Article

Computed tomographic appearance of lissencephaly syndromesDOBYNS, W. B; MCCLUGGAGE, C. W.American journal of neuroradiology. 1985, Vol 6, Num 4, pp 545-550, issn 0195-6108Article

Lissencephaly : a human brain maformation associated with deletion of the LIS1 gene located at chromosome 17p13DOBYNS, W. B; CARROZZO, R; LEDBETTER, D. H et al.JAMA, the journal of the American Medical Association. 1993, Vol 270, Num 23, pp 2838-2842, issn 0098-7484Article

Syndromes with lissencephaly. I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephalyDOBYNS, W. B; STRATTON, R. F; GREENBERG, F et al.American journal of medical genetics. 1984, Vol 18, Num 3, pp 509-526, issn 0148-7299Article

Mechanisms of interhemispheric transfer and patterns of cognitive function in acallosal patients of normal intelligenceFISCHER, M; RYAN, S. B; DOBYNS, W. B et al.Archives of neurology (Chicago). 1992, Vol 49, Num 3, pp 271-277, issn 0003-9942Article

Bilateral frontal polymicrogyria : A newly recognized brain malformation syndromeGUERRINI, R; BARKOVICH, A. J; SZTRIHA, L et al.Neurology. 2000, Vol 54, Num 4, pp 909-913, issn 0028-3878Article

Cerebello-oculo-renal syndromes including arima, senior-Löken and COACH syndromes : More than just variants of Joubert syndromeSATRAN, D; PIERPONT, M. E. M; DOBYNS, W. B et al.American journal of medical genetics. 1999, Vol 86, Num 5, pp 459-469, issn 0148-7299Article

Classical lissencephaly syndromes : does the face reflect the brain?ALLANSON, J. E; LEDBETTER, D. H; DOBYNS, W. B et al.Journal of medical genetics. 1998, Vol 35, Num 11, pp 920-923, issn 0022-2593Article

Idiopathic intracranial hypertension and facial diplegiaSELKY, A. K; DOBYNS, W. B; YEE, R. D et al.Neurology. 1994, Vol 44, Num 2, issn 0028-3878, p. 357Article

Periventricular heterotopia : phenotypic heterogeneity and correlation with Filamin A mutationsPARRINI, E; RAMAZZOTTI, A; BODELL, A et al.Brain. 2006, Vol 129, pp 1892-1906, issn 0006-8950, 15 p., 7Article

Megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus: A rare brain malformation syndrome associated with mental retardation and seizuresMIRZAA, G; DODGE, N. N; GLASS, I et al.Neuropediatrics. 2004, Vol 35, Num 6, pp 353-359, issn 0174-304X, 7 p.Article

Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain diseaseCORMAND, B; PIHKO, H; VOIT, T et al.Neurology. 2001, Vol 56, Num 8, pp 1059-1069, issn 0028-3878Article

Genetic and neuroradiological heterogeneity of double cortex syndromeGLEESON, J. G; LUO, R. F; SCHEFFER, I et al.Annals of neurology. 2000, Vol 47, Num 2, pp 265-269, issn 0364-5134Article

LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformationPILZ, D. T; MATSUMOTO, N; ROSS, M. E et al.Human molecular genetics (Print). 1998, Vol 7, Num 13, pp 2029-2037, issn 0964-6906Article

Rapid-onset dystonia-parkinsonism : A report of clinical, biochemical, and genetic studies in two familiesBRASHEAR, A; BUTLER, I. J; OZELIUS, L. J et al.Advances in neurology. 1998, Vol 78, pp 335-339, issn 0091-3952Conference Paper

A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3CHONG, S. S; PACK, S. D; ROSCHKE, A. V et al.Human molecular genetics (Print). 1997, Vol 6, Num 2, pp 147-155, issn 0964-6906Article

Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral refluxPHAIKASAME SANYANUSIN; SCHIMMENTI, L. A; MCNOE, L. A et al.Nature genetics. 1995, Vol 9, Num 4, pp 358-364, issn 1061-4036Article

Autosomal dominant optic nerve colobomas, vesicoureteral reflux, and renal anomaliesSCHIMMENTI, L. A; PIERPONT, M. E; CARPENTER, B. L. M et al.American journal of medical genetics. 1995, Vol 59, Num 2, pp 204-208, issn 0148-7299Article