The classification of cortical dysplasias through molecular genetics
- 1 September 2004
- journal article
- review article
- Published by Elsevier in Brain & Development
- Vol. 26 (6), 351-362
- https://doi.org/10.1016/s0387-7604(03)00093-7
Abstract
No abstract availableThis publication has 80 references indexed in Scilit:
- Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopiaEuropean Journal of Human Genetics, 2001
- Mutations in the human Sonic Hedgehog gene cause holoprosencephalyNature Genetics, 1996
- Proliferative events in the cerebral ventricular zoneBrain & Development, 1995
- A protein related to extracellular matrix proteins deleted in the mouse mutant reelerNature, 1995
- Familial schizencephalyBrain & Development, 1993
- Epilepsy and anomalies of neuronal migration: MRI and clinical aspectsActa Neurologica Scandinavica, 1992
- Holoprosencephaly in infants of diabetic mothersThe Journal of Pediatrics, 1983
- Miller-Dieker syndrome: Lissencephaly andmonosomy 17pThe Journal of Pediatrics, 1983
- Autosomal dominant microcephalyThe Journal of Pediatrics, 1979
- Hypothalamic-pituitary dysfunction in siblings of patients with holoprosencephalyThe Journal of Pediatrics, 1973