| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S1042-3680(18)30719-8 |
| P698 | PubMed publication ID | 1821304 |
| P2093 | author name string | Cohen MM Jr | |
| Kreiborg S | |||
| P2860 | cites work | Agenesis of the corpus callosum, combined immunodeficiency, bilateral cataract, and hypopigmentation in two brothers | Q28296474 |
| PRELIMINARY ANALYSIS OF FUNCTIONS OF THE TEMPORAL LOBES IN MONKEYS | Q29541597 | ||
| Agenesis of the corpus callosum in two brothers | Q30443069 | ||
| X linked recessive inheritance of agenesis of the corpus callosum | Q33670311 | ||
| Clinicopathological findings associated with agenesis of the corpus callosum. | Q34173689 | ||
| Corpus callosum agenesis, facial anomalies, Robin sequence, and other anomalies: a new autosomal recessive syndrome? | Q34686658 | ||
| The central nervous system in the Apert syndrome | Q38140616 | ||
| Agenesis of the corpus callosum: clinical, neuroradiological and cytogenetic studies | Q38188935 | ||
| Perspectives on holoprosencephaly: Part III. Spectra, distinctions, continuities, and discontinuities | Q38720465 | ||
| Agenesis of the corpus callosum: a study of the frequency of associated malformations | Q40061113 | ||
| Agenesis of the corpus callosum and gyral malformations are frequent manifestations of nonketotic hyperglycinemia | Q43803426 | ||
| Abnormalities of corpus callosum in patients with inherited metabolic diseases | Q43865656 | ||
| Bilateral and limited amygdalohippocampal lesions causing a pure amnesic syndrome | Q44087013 | ||
| Agenesis of the corpus callosum and limbic malformation in Apert syndrome (type I acrocephalosyndactyly). | Q48212624 | ||
| Spontaneous recurrent hypothermia accompanying agenesis of the corpus callosum | Q49080070 | ||
| Hydrocephalus and mental retardation in craniosynostosis. | Q52081305 | ||
| Agenesis of the corpus callosum and limbic malformations revisited | Q56397883 | ||
| Acrocallosal syndrome | Q68721293 | ||
| Agenesis of the corpus callosum: a marker for inherited metabolic disease? | Q69618081 | ||
| Agenesis of corpus callosum, ocular, and skeletal anomalies (X-linked dominant Aicardi's syndrome) in a girl with balanced X/3 translocation | Q71639110 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 565-568 | |
| P577 | publication date | 1991-07-01 | |
| P1433 | published in | Neurosurgery clinics of North America | Q26842825 |
| P1476 | title | Agenesis of the corpus callosum. Its associated anomalies and syndromes with special reference to the Apert syndrome | |
| P478 | volume | 2 |
| Q55032077 | Apert syndrome: A case report and review of the literature. |
| Q39326391 | Brain phenotypes in two FGFR2 mouse models for Apert syndrome |
| Q41111937 | Integration of Brain and Skull in Prenatal Mouse Models of Apert and Crouzon Syndromes |
| Q21092495 | NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects |
| Q34673186 | Novel molecular pathways elicited by mutant FGFR2 may account for brain abnormalities in Apert syndrome |
| Q54444041 | Postnatal brain and skull growth in an Apert syndrome mouse model. |
| Q48162522 | Prognostic indicators in the prenatal diagnosis of agenesis of corpus callosum |
| Q56334485 | [Classification of craniosynostosis] |
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