An Autosomal Recessive Form of Bilateral Frontoparietal Polymicrogyria Maps to Chromosome 16q12.2-21
- 1 April 2002
- journal article
- case report
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 70 (4), 1028-1033
- https://doi.org/10.1086/339552
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Malformations of cortical development and epilepsyBrain & Development, 2001
- Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopment.2000
- Allegro, a new computer program for multipoint linkage analysisNature Genetics, 2000
- Bilateral frontoparietal polymicrogyria and epilepsyPediatric Neurology, 2000
- Bilateral frontal polymicrogyriaNeurology, 2000
- Bilateral parasagittal parietooccipital polymicrogyria and epilepsyAnnals of Neurology, 1997
- A new autosomal recessive syndrome of pachygyriaClinical Genetics, 1996
- Congenital bilateral perisylvian syndrome: study of 31 patientsThe Lancet, 1993
- Homozygosity Mapping: A Way to Map Human Recessive Traits with the DNA of Inbred ChildrenScience, 1987
- Strategies for multilocus linkage analysis in humans.Proceedings of the National Academy of Sciences of the United States of America, 1984