Syndromes with lissencephaly.
Open Access
- 1 April 1996
- journal article
- review article
- Published by BMJ in Journal of Medical Genetics
- Vol. 33 (4) , 319-323
- https://doi.org/10.1136/jmg.33.4.319
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- Detecting deletions in the critical region for lissencephaly on 17p13.3 using fluorescent in situ hybridisation and a PCR assay identifying a dinucleotide repeat polymorphism.Journal of Medical Genetics, 1995
- Clinical spectrum and genetic studies of Fukuyama congenital muscular dystrophyAmerican Journal of Medical Genetics, 1994
- X‐linked pachygyria and agenesis of the corpus callosum: Evidence for an X chromosome lissencephaly locusAnnals of Neurology, 1994
- Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31–33Nature Genetics, 1993
- Walker-Warburg syndrome: Prenatal ultrasound findingsPrenatal Diagnosis, 1993
- Development of the cortical dysplasia of type II lissencephalyNeuropathology and Applied Neurobiology, 1993
- Muscle‐eye‐brain disease and Walker‐Warburg syndromeAmerican Journal of Medical Genetics, 1990
- Syndromes with lissencephaly. I: Millerdieker and Norman‐Roberts syndromes and isolated lissencephalyAmerican Journal of Medical Genetics, 1984
- A genetic study of the Fukuyama type congenital muscular dystrophyBrain & Development, 1984
- Miller-Dieker syndrome: Lissencephaly andmonosomy 17pThe Journal of Pediatrics, 1983