Confirmation of linkage of benign familial neonatal convulsions to D20S19 and D20S20
- 1 April 1992
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 89 (1) , 54-58
- https://doi.org/10.1007/bf00207042
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Benign familial neonatal convulsions: Evidence for clinical and genetic heterogeneityAnnals of Neurology, 1991
- Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region of chromosome 6American Journal of Medical Genetics, 1991
- Genes and epilepsy.Journal of Medical Genetics, 1990
- Proposal for Revised Classification of Epilepsies and Epileptic SyndromesEpilepsia, 1989
- Benign familial neonatal convulsions linked to genetic markers on chromosome 20Nature, 1989
- Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6American Journal of Medical Genetics, 1988
- Isolation and mapping of a polymorphic DNA sequence (pCMM6) on chromosome 20 [D20S19]Nucleic Acids Research, 1988
- A technique for radiolabeling DNA restriction endonuclease fragments to high specific activityAnalytical Biochemistry, 1983
- Proposal for Revised Clinical and Electroencephalographic Classification of Epileptic SeizuresEpilepsia, 1981
- Benign familial convulsions in the neonatal period and early infancyThe Journal of Pediatrics, 1979