Disease: Polysyndactyly trigonocephaly agenesis of corpus callosum
- A de novo GLI3 mutation in a patient with acrocallosal syndrome
- Agenesis of the corpus callosum and limbic malformation in Apert syndrome (type I acrocephalosyndactyly)
- Agenesis of the corpus callosum and limbic malformation in Apert's syndrome
- Agenesis of the corpus callosum and limbic malformations revisited
- Agenesis of the corpus callosum in Apert syndrome?
- Agenesis of the corpus callosum. Its associated anomalies and syndromes with special reference to the Apert syndrome
- Apert syndrome: what prenatal radiographic findings should prompt its consideration?
- Apert's syndrome with occipital encephalocele and absence of corpus callosum
- Brain malformation in syndromic craniosynostoses, a primary disorder of white matter: a review
- Central nervous system and cervical spine abnormalities in Apert syndrome
- Comparison of ultrasound and magnetic resonance imaging in the prenatal diagnosis of Apert syndrome: report of a case
- Computed tomography of abnormally shaped pediatric cranium
- Gastrointestinal disorders in Curry-Jones syndrome: Clinical and molecular insights from an affected newborn
- Magnetic resonance imaging in the malformative syndromes with mental retardation
- Metopic craniosynostosis due to mutations in GLI3: A novel association
- Olfactory bulb and olfactory tract abnormalities in acrocallosal syndrome and Greig cephalopolysyndactyly syndrome
- Pfeiffer-like syndrome with holoprosencephaly: a newborn with maternal smoking and alcohol exposure
- Polysyndactyly and trigonocephaly with partial agenesis of corpus callosum
- Polysyndactyly and trigonocephaly with partial agenesis of corpus callosum: an example of the variable clinical spectrum of the Acrocallosal syndrome?
- Psychosis in Apert's syndrome with partial agenesis of the corpus callosum
- Selected clinical research involving the central nervous system
- The central nervous system in the Apert syndrome
- Variant type and position predict two distinct limb phenotypes in patients with GLI3-mediated polydactyly syndromes